Wikidata:Database reports/Constraint violations/P557

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Constraint violations report for DiseasesDB (Discussion, uses, items, changes, related properties): identifier sourced on the Diseases Database
Data time stamp: (UTC) — Items processed: 3,140
The report is generated based on the settings on Property:P557#P2302.
Updates overwrite this page. Some may already be fixed since the last update: check RecentChangesLinked.
When incremental dumps and the bot work as planned, items fixed before 07:00 UTC disappear in the next update. The report is not updated if only the item count changes.
The report can include false positives. There is no need to "fix" them.

"Single value" violations[edit]

Violations count: 70

"Type physiological condition (Q7189713), disease (Q12136)" violations[edit]

Violations count: 56

Types statistics[edit]

Accepted Type Usage
Yes disease (Q12136) 1442
Yes rare disease (Q929833) 718
Yes developmental defect during embryogenesis (Q55788864) 249
Yes infectious disease (Q18123741) 231
Yes designated intractable/rare disease (Q42303753) 214
Yes syndrome (Q179630) 174
Yes genetic disease (Q200779) 147
Yes autosomal dominant disease (Q18553439) 114
Yes autosomal recessive disease (Q10267817) 109
Yes clinical sign (Q1441305) 99
Yes skin disease (Q949302) 77
Yes head and neck disease (Q55789477) 65
Yes viral infectious disease (Q1928978) 55
Yes symptom (Q169872) 50
Yes primary bacterial infectious disease (Q18553247) 37
Yes health problem (Q2057971) 36
Yes inflammatory disease (Q3508753) 35
Yes lung disease (Q3392853) 33
Yes immune disorder (Q3843811) 30
Yes amino acid metabolic disorder (Q18558086) 29
Yes osteochondrodysplasia (Q3251367) 29
Yes rare genetic developmental defect during embryogenesis (Q55785846) 29
Yes congenital disorder (Q727096) 29
Yes eye disease (Q3041498) 28
Yes neurometabolic disease (Q1337418) 28
Yes kidney disease (Q1054718) 26
Yes intestinal disease (Q3055380) 25
Yes parasitic helminthiasis infectious disease (Q578994) 25
Yes genetic syndromic intellectual disability (Q55785866) 25
Yes arthropathy (Q708176) 24
Yes bacterial infectious disease (Q727028) 24
Yes encephalopathy (Q576349) 24
Yes notifiable disease (Q314676) 24
Yes zoonosis (Q182672) 23
Yes X-linked recessive disease (Q55010090) 23
Yes syndromic developmental defect of the eye (Q55785336) 22
Yes multiple congenital anomalies/dysmorphic syndrome-intellectual disability (Q55785288) 22
Yes nervous system heredodegenerative disease (Q19001236) 22
No taxon (Q16521) 20
Yes genetic nervous system disorder (Q55788492) 20
Yes neurological disorder (Q3339235) 19
Yes rare genetic epilepsy (Q55785842) 19
Yes developmental anomaly of metabolic origin (Q55785399) 18
Yes autoimmune disease (Q8084905) 18
Yes eye degenerative disease (Q18558225) 18
Yes multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome (Q55785289) 17
Yes bone disease (Q4941552) 17
Yes thoracic disease (Q18553676) 17
Yes multiple congenital anomalies/dysmorphic syndrome without intellectual disability (Q55785290) 16
Yes neglected tropical disease (Q929451) 16
Yes liver disease (Q929737) 16
Yes syndromic renal or urinary tract malformation (Q55788832) 16
Yes connective tissue disease (Q1779300) 16
Yes occupational disease (Q637816) 15
Yes skin and integumentary tissue symptom (Q100751718) 15
Yes secondary glomerular disease (Q55788835) 15
Yes chromosomal deletion syndrome (Q16918398) 15
Yes rare genetic respiratory disease (Q55785522) 15
Yes esophageal disease (Q2912193) 15
Yes congenital heart disease (Q939364) 15
Yes physiological condition (Q7189713) 15
Yes muscular disease (Q692536) 14
Yes polymalformative genetic syndrome with increased risk of developing cancer (Q55785832) 14
Yes neurodegeneration (Q1755122) 14
Yes carbohydrate metabolic disorder (Q6013981) 13
Yes pain (Q81938) 13
Yes vascular disease (Q1266890) 13
Yes hereditary disorder (Q3311537) 12
Yes syndromic genetic deafness (Q55788734) 12
Yes movement disorders (Q2608695) 12
Yes inherited blood coagulation disease (Q18555031) 12
Yes monogenic disease (Q1225194) 12
Yes central nervous system disease (Q5062122) 12
Yes skin infection (Q2458539) 12
Yes genetic skin vascular disorder (Q55785835) 12
Yes nail disease (Q2084035) 11
Yes heart disease (Q190805) 11
Yes fungal infectious disease (Q464067) 11
Yes inherited metabolic disorder (Q1758393) 11
Yes autosomal genetic disease (Q18553442) 11
Yes gastrointestinal system disease (Q2300099) 11
Yes glycogen storage disease (Q1421738) 11
Yes lipid metabolism disorder (Q1476525) 11
Yes respiratory signs and symptoms (Q42183538) 11
Yes spinal disease (Q7577457) 11
Yes X-linked intellectual disability (Q8041560) 11
Yes ectodermal dysplasia (Q1323713) 11
Yes mental disorder (Q12135) 11
Yes hemic system symptom (Q102186671) 11
Yes inflammation (Q101991) 11
Yes autoimmune disease of musculoskeletal system (Q18553609) 11
Yes rare skin disease (Q55788696) 11
Yes eyelid disease (Q18556729) 11
Yes mouth disease (Q2508462) 11
Yes vascular skin disease (Q18558156) 11
Yes commensal bacterial infectious disease (Q18553248) 10
Yes malformation syndrome with skin/mucosae involvement (Q55785402) 10
Yes foot diseases (Q5282137) 10
Yes hair diseases (Q2989168) 10
Yes benign neoplasms by histologic type (Q18553645) 10
Yes penile disease (Q18554834) 10
Yes retinal disease (Q550455) 10
Yes blood coagulation disease (Q890200) 10
Yes skin tumor or hamartoma (Q55788604) 10
Yes chromosomal disease (Q4501577) 10
Yes endemic disease (Q506680) 10
Yes female reproductive system disease (Q5442760) 9
Yes complications of pregnancy (Q2916477) 9
Yes peripheral vascular disease (Q26695607) 9
Yes pigmentation disorder (Q7193408) 9
Yes injury (Q193078) 9
Yes cyst (Q193211) 9
Yes parasitic protozoa infectious disease (Q353172) 9
Yes autoimmune skin disease (Q12504769) 9
Yes overgrowth syndrome (Q7113674) 9
Yes arthritis (Q170990) 9
Yes lysosomal storage disease with skeletal involvement (Q55788818) 9
Yes hematopoietic system disease (Q1963588) 9
Yes erythema (Q1166142) 9
Yes cardiovascular system symptom (Q102186826) 9
Yes keratosis (Q3667186) 9
Yes bullous skin disease (Q18557957) 9
Yes bone inflammation disease (Q1178507) 9
Yes hereditary retinal dystrophy (Q18557955) 9
Yes testicular disease (Q7705854) 9
Yes syndromic dyslipidemia (Q55785804) 9
Yes spinal cord disease (Q2303951) 9
Yes malformation syndrome with short stature (Q55785400) 9
Yes dermatitis (Q229256) 9
Yes congenital disorder of amino acid metabolism (Q3281372) 8
Yes metabolic disease (Q2351083) 8
Yes syndromic anorectal malformation (Q55785353) 8
Yes neurological and physiological symptom (Q99860490) 8
Yes respiratory disease (Q3286546) 8
Yes bladder disease (Q6066379) 8
Yes infectious disease of the nervous system (Q10336461) 8
Yes rare genetic endocrine disease (Q55785525) 8
Yes neurological symptom (Q12040808) 8
Yes sexually transmitted infection (Q12198) 8
Yes metal metabolism disorder (Q3281373) 8
Yes gastrointestinal system cancer (Q5526839) 8
Yes peripheral neuropathy (Q945238) 8
Yes opportunistic mycosis (Q18555090) 8
Yes nutritional deficiency disease (Q1890194) 8
Yes eye symptom (Q102186610) 8
Yes breast disease (Q4959796) 8
Yes nephropathy secondary to a storage or other metabolic disease (Q55788855) 8
Yes tick-borne disease (Q184243) 8
Yes muscular dystrophy (Q1137767) 8
Yes rare metabolic liver disease (Q55785261) 8
Yes vaginal disease (Q18211693) 8
Yes renal tubular transport disease (Q6013986) 7
Yes anthroponotic disease (Q1049711) 7
Yes thyroid gland disease (Q6673122) 7
Yes syndromic obesity (Q55786310) 7
Yes diabetes (Q12206) 7
Yes cerebral degeneration (Q1620193) 7
Yes aortic disease (Q18556675) 7
Yes rare genetic vascular tumor (Q55788290) 7
Yes colonic disease (Q18556754) 7
Yes male reproductive system disease (Q6742925) 7
Yes ectoparasitism (Q5334259) 7
Yes ptosis (Q622427) 7
Yes ichthyosis (Q523893) 7
Yes anal disease (Q56603543) 7
Yes pneumoconiosis (Q651223) 7
Yes progeroid syndrome (Q6139748) 7
Yes lysosomal storage disease (Q675010) 7
Yes hereditary neoplastic syndromes (Q1348398) 7
Yes eye inflammation (Q2971524) 7
Yes optic nerve disease (Q2879095) 7
Yes photodermatosis (Q2986815) 7
Yes arbovirosis (Q2859732) 7
Yes rare rheumatologic disease (Q55785828) 7
Yes rare nervous system tumor (Q55789072) 7
Yes syndromic glaucoma (Q55789219) 7
Yes urinary system disease (Q7900883) 7
Yes brain cancer (Q9303627) 7
Yes classic organic aciduria (Q55788539) 7
Yes vein disorder (Q7918687) 7
Yes placenta disease (Q7200296) 7
Yes leukocyte disease (Q18558143) 7
Yes palmoplantar keratosis (Q7128426) 7
Yes pancreas disease (Q7130407) 7
Yes hypertrophic cardiomyopathy (Q1364270) 7
Yes heart conduction disease (Q1361515) 7
Yes infectious disease with epilepsy (Q55785635) 7
Yes urological symptom (Q2565950) 7
Yes reproductive system symptom (Q102186786) 7
Yes other acquired skin disease (Q55788714) 7
Yes rare genetic immune disease (Q55785867) 7
Yes cestodosis (Q4505372) 6
Yes syndromic neurometabolic disease with X-linked intellectual disability (Q55785814) 6
Yes gallbladder disease (Q5518905) 6
Yes skin benign neoplasm (Q18555315) 6
Yes orofacial clefting syndrome (Q55785405) 6
Yes syndrome or malformation associated with head and neck malformations (Q55785513) 6
Yes inner ear disease (Q18555242) 6
Yes strabismus (Q179951) 6
Yes mucopolysaccharidosis (Q1479681) 6
Yes sleep disorder (Q177190) 6
Yes organic acidemia (Q1547640) 6
Yes baldness (Q181391) 6
Yes endocrine gland cancer (Q18554878) 6
Yes X-linked dominant disease (Q55010089) 6
Yes emphysema (Q1339243) 6
Yes central nervous system and retinal vascular disease (Q55788489) 6
Yes foot deformity (Q5465742) 6
Yes bone development disease (Q18553737) 6
Yes metabolic disease with cataract (Q55789275) 6
Yes metabolic disease with corneal opacity (Q55789274) 6
Yes mitochondrial disease with eye involvement (Q55789259) 6
Yes unclassified primitive or secondary maculopathy (Q55789241) 6
Yes syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy (Q55787048) 6
Yes sex differentiation disease (Q18554938) 6
Yes mineral deficiency (Q16944888) 6
Yes rare genetic bone disease (Q55785844) 6
Yes stomach disease (Q175827) 6
Yes metabolic disease with intestinal involvement (Q55785312) 6
Yes cervix disease (Q18555046) 6
Yes autoinflammatory syndrome with skin involvement (Q55787013) 6
Yes glomerulonephritis (Q605006) 6
Yes genetic peripheral neuropathy (Q55789138) 6
Yes cyanotic heart defect (Q2186829) 6
Yes animal disease (Q9190427) 6
Yes tongue disease (Q7107436) 6
Yes reactive neutrophilic dermatose (Q7300315) 6
Yes foodborne illness (Q272002) 6
Yes waterborne disease (Q2006636) 6
Yes vitamin deficiency (Q194435) 6
Yes knee disorder (Q18971535) 6
Yes lymphoproliferative disorders (Q4165484) 6
Yes neoplasm (Q1216998) 6
Yes visual impairment (Q737460) 6
Yes connective tissue neoplasm (Q3542012) 6
Yes mucinosis (Q6931138) 6
Yes artery disease (Q18965518) 6
Yes hemangioma (Q861028) 6
Yes eating disorder (Q373822) 6
Yes specific developmental disorder (Q7574983) 6
Yes cellulitis (Q876887) 6
Yes Herpesviridae infectious disease (Q18975237) 6
Yes motor neuron disease (Q3221083) 6
Yes leukocytosis (Q974869) 6
Yes osteochondrosis (Q1154055) 6
Yes flavivirus infectious disease (Q19001421) 6
Yes upper respiratory tract disease (Q18558209) 6
Yes nematode infection (Q2072680) 6
Yes interstitial lung disease (Q1153419) 6
Yes rickettsiosis (Q646664) 6
Yes uterine disease (Q18555940) 6
Yes vasculitis (Q644318) 6
Yes rare intoxication (Q55785342) 5
Yes intrinsic cardiomyopathy (Q18553611) 5
Yes non-syndromic respiratory or mediastinal malformation (Q55785339) 5
Yes cell type cancer (Q18553402) 5
Yes autoimmune disease of peripheral nervous system (Q18553610) 5
Yes myositis (Q1433212) 5
Yes rare genetic eye disease (Q55785254) 5
Yes syndromic diaphragmatic or abdominal wall malformation (Q55785334) 5
Yes heart arrhythmia (Q189331) 5
Yes primary immunodeficiency disease (Q3043160) 5
Yes rare acquired eye disease (Q55785265) 5
Yes spotted fever (Q9274700) 5
Yes sphingolipidosis (Q2309612) 5
Yes channelopathy (Q2936142) 5
Yes thrombophilia (Q1570013) 5
Yes lymph node disease (Q18558262) 5
Yes leukodystrophy (Q1821559) 5
Yes acrocephalosyndactylia (Q1786496) 5
Yes type 2 collagen-related bone disorder (Q55788797) 5
Yes coronary artery disease (Q844935) 5
Yes corneal disease (Q10526382) 5
Yes respiratory system abnormality (Q18975820) 5
Yes complication of pregnancy, childbirth and the puerperium (Q18975815) 5
Yes atypical pneumonia (Q2633267) 5
Yes rare abdominal surgical disease (Q55785601) 5
Yes inflammatory and autoimmune disease with epilepsy (Q55785633) 5
Yes alopecia (Q2697787) 5
Yes amyloidosis (Q816798) 5
Yes major trauma (Q1064904) 5
Yes filariasis (Q815753) 5
Yes porphyria (Q271759) 5
Yes tyrosinemia (Q1122668) 5
Yes head and neck cancer (Q1783924) 5
Yes rare syndrome with cardiac malformations (Q55785518) 5
Yes type IV hypersensitivity (Q7860879) 5
Yes colitis (Q2453464) 5
Yes perinatal disease (Q18968218) 5
Yes bronchospasm (Q279330) 5
Yes urination disorder (Q19000619) 5
Yes acidosis (Q185089) 5
Yes vision disorder (Q767669) 5
Yes splenic disease (Q7578540) 5
Yes dermatophytosis (Q1909343) 5
Yes collagen disease (Q1446169) 5
Yes headache (Q86) 5
Yes atresia (Q757722) 5
Yes congenital hemolytic anemia (Q5160435) 5
Yes mitochondrial disease with dilated cardiomyopathy (Q55786150) 5
Yes mitochondrial disease with epilepsy (Q55786197) 5
Yes neuroendocrine tumor (Q1981276) 5
Yes pseudohermaphroditism (Q2273662) 5
Yes skin hemangioma (Q18556451) 5
Yes mitochondrial disease with peripheral neuropathy (Q55786198) 5
Yes genetic otorhinolaryngologic disease (Q55788308) 5
Yes pityriasis (Q2097389) 5
Yes facial nerve disease (Q18554894) 5
Yes viral hemorrhagic fever (Q162272) 5
Yes mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA (Q55786430) 5
Yes bile duct disease (Q18556206) 5
Yes nervous system malformations (Q584265) 5
Yes viral hepatitis (Q1983841) 5
Yes lymphatic system disease (Q6708237) 5
Yes hypersensitivity (Q5958765) 5
Yes childhood cancer (Q5097977) 5
Yes arterial hypertension (Q41861) 5
Yes porphyria due to ALAD deficiency (Q419897) 5
Yes metal poisoning (Q4215775) 5
Yes mycobacterium infectious disease (Q4293079) 5
Yes allergy (Q42982) 5
Yes iron overload (Q2025687) 5
Yes encephalomyelitis (Q1634879) 5
Yes dysostosis (Q1269307) 5
Yes amino acid transport disorder (Q471778) 5
Yes urethral disease (Q18557550) 5
Yes genetic neurodegenerative disease with dementia (Q55346116) 5
Yes hemolytic anemia (Q1145668) 5
Yes acquired metabolic disease (Q18553699) 5
Yes ovarian disease (Q7113244) 5
Yes metabolic disease with pigmentary retinitis (Q55789276) 5
Yes inherited renal tumor (Q55785849) 5
Yes rare genetic gynecological and obstetrical diseases (Q55785863) 5
Yes anemia (Q5445) 5
Yes salivary gland disease (Q17152566) 5
Yes lysosomal disease with hypertrophic cardiomyopathy (Q55786143) 5
Yes syndrome associated with hypertrophic cardiomyopathy (Q55786146) 5
Yes mosquito-borne disease (Q6916469) 5
Yes digestive sign (Q54926352) 5
Yes organic brain syndrome (Q360341) 5
Yes parasitic skin disease (Q54911414) 5
Yes autonomic nervous system disease (Q18554088) 5
Yes blood platelet disease (Q2429620) 4
Yes pyoderma (Q2119633) 4
Yes hypothyroidism (Q16501) 4
Yes syndrome with disorder of sex development of gynecological interest (Q55787661) 4
Yes pelvic organ prolapse (Q166102) 4
Yes disorder of glycolysis (Q55787283) 4
Yes hemoglobinopathy (Q1642147) 4
Yes sarcoma (Q223911) 4
Yes infarction (Q207550) 4
Yes genetic central nervous system and retinal vascular disease (Q55785839) 4
Yes hospital-acquired infection (Q215509) 4
Yes valve insufficiency (Q22977956) 4
Yes autoimmune connective tissue disorder (Q2208472) 4
Yes menstrual disorder (Q2137327) 4
Yes systemic inflammatory disease associated with an acquired peripheral neuropathy (Q55785994) 4
Yes tachycardia (Q209583) 4
Yes copper metabolism disease (Q19001238) 4
Yes syndromic diaphragmatic or thoracic malformation (Q55785792) 4
Yes deficient breast volume or number (Q55785775) 4
Yes calcinosis (Q239027) 4
Yes Huntington's disease-like syndrome (Q24977062) 4
Yes autoimmune disease of the nervous system (Q18556300) 4
Yes bone structure disease (Q18553740) 4
Yes lipid storage disease (Q3540902) 4
Yes blood protein disease (Q18557170) 4
Yes extrinsic allergic alveolitis (Q35890) 4
Yes central nervous system vascular malformation (Q54945930) 4
Yes neural tube defect (Q548213) 4
Yes congenital adrenal hyperplasia (Q366868) 4
Yes dermatomycosis (Q3705876) 4
Yes anxiety disorder (Q544006) 4
Yes corneal degeneration (Q18554311) 4
Yes sweat gland disease (Q18554617) 4
Yes craniosynostosis (Q378183) 4
Yes chronic condition (Q383126) 4
Yes bilirubin metabolic disorder (Q390475) 4
Yes carcinoma (Q33525) 4
Yes bone cancer (Q18554919) 4
Yes glucose metabolism disease (Q18556224) 4
Yes epilepsy (Q41571) 4
Yes combined immunodeficiency (Q5150906) 4
Yes neuronal ceroid lipofuscinosis (Q4358039) 4
Yes central nervous system viral disease (Q5062121) 4
Yes iris disease (Q18555070) 4
Yes genetic epidermal disorder (Q55785833) 4
Yes adverse drug reaction (Q45959) 4
Yes refractive error (Q470427) 4
Yes coccidiosis (Q487837) 4
Yes autoimmune disease of cardiovascular system (Q4826340) 4
Yes meningitis (Q48143) 4
Yes abnormal skin coloration (Q47085690) 4
Yes superficial mycosis (Q18928094) 4
Yes chromosomal anomaly with epilepsy as a major feature (Q55785627) 4
Yes psoriasis (Q179945) 4
Yes dissection (Q2660911) 4
Yes adenoma (Q272741) 4
Yes coagulation factor deficiency (Q18971506) 4
Yes venous thrombosis (Q2751330) 4
Yes predominantly large-vessel vasculitis (Q55785504) 4
Yes syndromic craniosynostosis (Q55785407) 4
Yes subcutaneous mycosis (Q18553213) 4
Yes primary systemic mycosis (Q18553244) 4
Yes perinatal respiratory disorder (Q18966634) 4
Yes horse disease (Q29568408) 4
Yes cerebrovascular disease (Q3010352) 4
Yes retinal degeneration (Q3043268) 4
Yes periodic paralysis (Q1788314) 4
Yes cognitive disorder (Q3065932) 4
Yes rare dyslipidemia (Q55785266) 4
Yes syndromic intellectual disability (Q18553536) 4
Yes general symptom (Q31836626) 4
Yes genetic cardiac rhythm disease (Q55785258) 4
Yes autoimmune disease of gastrointestinal tract (Q18553608) 4
Yes vitreous disease (Q18558199) 4
Yes breast benign neoplasm (Q18553643) 4
Yes peroxisomal disease (Q3281322) 4
Yes connective tissue benign neoplasm (Q18553680) 4
Yes inborn errors of purine–pyrimidine metabolism (Q3281375) 4
Yes bone remodeling disease (Q18553736) 4
Yes autosomal recessive metabolic cerebellar ataxia (Q55346092) 4
Yes bowel obstruction (Q16244733) 4
Yes pleural effusion (Q1334541) 4
Yes mitochondrial disease (Q935710) 4
Yes severe combined immunodeficiency (Q1334408) 4
Yes syndromic lymphedema (Q55788697) 4
Yes long QT syndrome (Q653924) 4
Yes rare bone disease (Q55788795) 4
Yes paraneoplastic syndrome (Q936417) 4
Yes abdominal symptom (Q102187028) 4
Yes primary bone dysplasia with increased bone density (Q55788814) 4
Yes color blindness (Q133696) 4
Yes obstetric labor complication (Q7075540) 4
Yes hypertension (Q95566669) 4
Yes feces and droppings symptom (Q102186864) 4
Yes geonosis (Q1503299) 4
Yes abnormality of red blood cells (Q5670888) 4
Yes porokeratosis (Q7230264) 4
Yes malformation syndrome (Q1401195) 4
Yes psychopathological syndrome (Q56815734) 4
Yes rare respiratory disease (Q55789042) 4
Yes transmissible spongiform encephalopathy (Q703961) 4
Yes isolated genetic hair shaft abnormality (Q55788586) 4
Yes heart valve stenosis (Q123482454) 4
Yes epidermal disease (Q55788577) 4
Yes osteosclerosis (Q1233526) 4
Yes pituitary gland disease (Q7199538) 4
Yes oligosaccharidosis (Q55788568) 4
Yes epidermolysis bullosa (Q923020) 4
Yes urea cycle disorder (Q1585743) 4
Yes Poxviridae infectious disease (Q12353899) 4
Yes bartonellosis (Q809561) 4
Yes musculoskeletal system symptom (Q102187380) 4
Yes rhinitis (Q114085) 4
Yes complication (Q1346149) 4
Yes respiratory failure (Q767485) 4
Yes panniculitis (Q780629) 4
Yes other dermis disorder (Q55788600) 4
Yes spinocerebellar ataxia (Q899726) 4
Yes Pigmented purpuric dermatosis (Q7193411) 4
Yes pregnancy with abortive outcome (Q96649463) 4
Yes vascular malformation (Q121576) 4
Yes dysostosis of genetic origin with limb anomaly as a major feature (Q55788097) 4
Yes nevus (Q692077) 4
Yes sensation perception (Q102186648) 4
Yes stroke (Q12202) 4
Yes puerperal disorders (Q7258523) 4
Yes demyelinating disease (Q1186703) 4
Yes malformation syndrome with hamartosis (Q55789095) 4
Yes genetic cardiac disease (Q55789068) 4
Yes nose symptom (Q102186674) 4
Yes women's disease (Q1451794) 4
Yes systemic disease (Q1414805) 4
Yes hemolytic anemia due to a disorder of glycolytic enzymes (Q55789127) 4
Yes calculus (Q617079) 4
Yes congenital muscular dystrophy (Q1321884) 4
Yes Intervertebral disc disorder (Q6057394) 4
Yes pemphigus (Q1483214) 4
Yes metabolic disease with dementia (Q55789148) 4
Yes poisoning (Q114953) 4
Yes trisomy (Q844903) 4
Yes deafness (Q12133) 4
Yes myeloid neoplasm (Q18553734) 3
Yes primary glomerular disease (Q55785293) 3
Yes tricuspid valve disease (Q18553500) 3
Yes dementia (Q83030) 3
Yes neoplastic syndrome (Q55789476) 3
Yes syndromic epicanthus (Q55789170) 3
Yes vitamin metabolic disorder (Q18553423) 3
Yes lichen disease (Q28026070) 3
Yes intestinal disease due to fat malabsorption (Q55785307) 3
Yes urinary incontinence (Q281490) 3
Yes endometrial disease (Q18553772) 3
Yes GM2 gangliosidosis (Q5513691) 3
Yes childhood electroclinical syndrome (Q18553414) 3
Yes secondary ectropion (Q55789166) 3
Yes lice infestation (Q1343674) 3
Yes parathyroid gland disease (Q7136145) 3
Yes endocrine organ benign neoplasm (Q18553650) 3
Yes rare gastroesophageal disease (Q55785259) 3
Yes autoimmune disease of endocrine system (Q18553586) 3
Yes lens shape anomaly (Q55789234) 3
Yes fibromatosis (Q1410851) 3
Yes fetopathy (Q1409154) 3
Yes poliomyelitis (Q12195) 3
Yes pelvic pain (Q7161805) 3
Yes retinal vascular disease (Q12195125) 3
Yes peritoneal disease (Q54935444) 3
Yes syndrome with a symptomatic strabismus (Q55789247) 3
Yes cheilitis (Q1068997) 3
Yes exostosis (Q1384176) 3
Yes trophoblastic neoplasm (Q7845637) 3
Yes Enterobacteriaceae infectious disease (Q18975069) 3
Yes male reproductive organ cancer (Q18556093) 3
Yes genodermatosis (Q666075) 3
Yes brain inflammatory disease (Q55785279) 3
Yes infection of the central nervous system (Q4316437) 3
Yes nervous system anomaly with eye involvement (Q55789255) 3
Yes urticarial syndrome (Q7901363) 3
Yes pneumonia (Q12192) 3
Yes ectodermal malformation syndrome associated with ocular features (Q55789272) 3
Yes pervasive developmental disorder (Q6691991) 3
Yes ischemic bone disease (Q26695332) 3
Yes embolism (Q275466) 3
Yes neuroacanthocytosis (Q746781) 3
Yes reproductive system disease (Q7314317) 3
Yes non-Langerhans-cell histiocytosis (Q3136521) 3
Yes kidney failure (Q476921) 3
Yes nasal cavity disease (Q18555020) 3
Yes streptococcal infection (Q5849703) 3
Yes complement deficiency (Q5156409) 3
Yes dysmelia (Q1269288) 3
Yes sex chromosome disorder (Q7458487) 3
Yes hypolipoproteinemia (Q5959735) 3
Yes skull cancer (Q18554923) 3
Yes intraabdominal infection (Q30314067) 3
Yes distomatosis (Q3030745) 3
Yes phakomatosis (Q748376) 3
Yes alphavirus infections (Q4735280) 3
Yes integumentary system disease (Q18554850) 3
Yes craniofacial abnormality (Q5182137) 3
Yes atrioventricular block (Q300121) 3
Yes viral encephalitis (Q3053951) 3
Yes fasciitis (Q1870975) 3
Yes B-cell lymphoma (Q4833719) 3
Yes psychopathological symptom (Q30897648) 3
Yes hepatic vascular disease (Q18555173) 3
Yes urticaria (Q187440) 3
Yes rare genetic disorder with obstructive azoospermia (Q55788066) 3
Yes leukopenia (Q496812) 3
Yes intoxication (Q18621601) 3
Yes Cutaneous perforating disorders (Q5196708) 3
Yes lupus erythematosus (Q188297) 3
Yes mood disorder (Q188638) 3
Yes zygomycosis (Q3046374) 3
Yes renal vascular disease (Q18555068) 3
Yes pupil disorder (Q18555067) 3
Yes iron metabolism disease (Q6072985) 3
Yes fatty liver disease (Q6058862) 3
Yes acute viral respiratory tract infection (Q55790495) 3
Yes female reproductive organ cancer (Q18554220) 3
Yes schizophrenia spectrum disorder (Q2903417) 3
Yes bone sarcoma (Q56014469) 3
Yes pleural disease (Q7204732) 3
Yes abnormal pupillary function (Q18554099) 3
Yes benign epithelial neoplasm (Q55790925) 3
Yes secondary neoplasm (Q55790826) 3
Yes viral skin disease (Q54911470) 3
Yes adrenal gland disease (Q4684717) 3
Yes congenital physical abnormality (Q3281904) 3
Yes diseases in twins (Q54943950) 3
Yes malformation of cortical development, Group I (Q54943988) 3
Yes lens disease (Q18553990) 3
Yes galactosemia (Q774483) 3
Yes post-viral disorder (Q55789779) 3
Yes Bunyaviridae infectious disease (Q18967528) 3
Yes gonadal dysgenesis (Q1332427) 3
Yes jaw disease (Q47108021) 3
Yes carotid artery disease (Q18555923) 3
Yes tooth pathology (Q5259414) 3
Yes IgG4-related disease (Q11039483) 3
Yes advers effect of psychopharmacological medication (Q62665995) 3
Yes ureteral disease (Q18554726) 3
Yes disorder of sex development (Q5282521) 3
Yes lacrimal apparatus disease (Q18554657) 3
Yes malformations of cortical development, Group III (Q55003193) 3
Yes treponematosis (Q1243869) 3
Yes classic venereal disease (Q56369564) 3
Yes sheep disease (Q53582403) 3
Yes coxsackievirus infectious disease (Q18966421) 3
Yes capillary disease (Q18554363) 3
Yes skin carcinoma (Q18555943) 3
Yes keratitis (Q757838) 3
Yes impulse control disorder (Q1201835) 3
Yes syndrome associated with dilated cardiomyopathy (Q55786153) 3
Yes ear symptom (Q102187283) 3
Yes somatoform disorder (Q936549) 3
Yes neuro-cardio-facial-cutaneous syndromes (Q17074582) 3
Yes amino acid or protein metabolism disease with epilepsy (Q55786194) 3
Yes mucolipidosis (Q1952032) 3
Yes other genetic dermis disorder (Q55788349) 3
Yes rare disease with malignant hyperthermia (Q55788310) 3
Yes rare hemorrhagic disorder due to a constitutional coagulation factors defect (Q55788455) 3
Yes bovine disease (Q3473026) 3
Yes inherited nervous system cancer-predisposing syndrome (Q55786407) 3
Yes overnutrition (Q16956975) 3
Yes heart septal defect (Q16934669) 3
Yes throat symptom (Q102186813) 3
Yes bone fracture (Q68833) 3
Yes Polysomy of X chromosome (Q55786716) 3
Yes acariasis (Q337998) 3
Yes sebaceous gland disease (Q18558062) 3
Yes muscle symptom (Q102187423) 3
Yes functional neutrophil defect (Q55785861) 3
Yes muscular channelopathy (Q55788493) 3
Yes inherited gynecological tumor (Q55785864) 3
Yes catecholamine-producing tumor (Q55788491) 3
Yes anti-neutrophil cytoplasmic antibody-associated vasculitis (Q17239200) 3
Yes aplastic anemia (Q846316) 3
Yes hyperostosis (Q1632552) 3
Yes purpura (Q935293) 3
Yes muscular glycogenosis (Q55785945) 3
Yes parasitic infectious diseases (Q1601794) 3
Yes genetic vascular anomaly (Q55786073) 3
Yes neurodevelopmental disorder (Q3450985) 3
Yes mitochondrial disease with hypertrophic cardiomyopathy (Q55786144) 3
Yes typhus (Q160649) 3
Yes abscess (Q164655) 3
Yes infection (Q166231) 3
Yes mitral valve disease (Q18557136) 3
Yes bacterial skin disease (Q11864371) 3
Yes constitutional neutropenia with extra-hematopoietic manifestations (Q55787695) 3
Yes aortic valve disease (Q18557169) 3
Yes somatosensory disorder (Q1641015) 3
Yes thyroiditis (Q11835644) 3
Yes ciliopathy (Q203031) 3
Yes vector-borne disease (Q2083837) 3
Yes hearing disorder (Q1644260) 3
Yes muscle tissue disease (Q18557307) 3
Yes rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin (Q55788068) 3
Yes osteochondrosis of genetic origin (Q55788022) 3
Yes postinfectious encephalitis (Q11830340) 3
Yes rare male fertility disorder with obstructive azoospermia (Q55788042) 3
Yes ovarian neoplasm (Q11793790) 3
Yes borreliosis (Q16006998) 3
Yes acyl-CoA dehydrogenase deficiency (Q55787302) 3
Yes degeneration of macula and posterior pole (Q16678480) 3
Yes disorder of fructose metabolism (Q55787284) 3
Yes genetic otorhinolaryngological malformation (Q55788178) 3
Yes lymphoma (Q208414) 3
Yes syndrome with limb reduction defects (Q55787046) 3
Yes encephalitis (Q199615) 3
Yes autoinflammatory syndrome with immune deficiency (Q55787012) 3
Yes polyposis (Q2103081) 3
Yes systemic diseases with anterior uveitis (Q55786944) 3
Yes multiple hamartoma syndrome (Q3508737) 3
Yes genetic systemic or rheumatologic disease (Q55786852) 3
Yes inherited digestive tract tumor (Q55786847) 3
Yes lymphatic system symptom (Q102186753) 3
Yes nerve compression syndrome (Q1978084) 3
Yes agammaglobulinemia (Q1047559) 3
Yes vitamin B deficiency (Q19001111) 3
Yes synucleinopathy (Q2376264) 3
Yes pemphigoid (Q881811) 3
Yes epilepsy syndrome (Q55785625) 3
Yes dysostosis with predominant vertebral and costal involvement (Q55788823) 3
Yes proliferative glomerulonephritis (Q18556474) 3
Yes patellar dysostosis (Q55788824) 3
Yes agenesis (Q392604) 3
Yes orbital disease (Q18558098) 3
Yes vulvar disease (Q18211751) 3
Yes chondropathy (Q851693) 3
Yes odontogenic tumor (Q7077953) 3
Yes genetic hypertension (Q55785524) 3
Yes genetic biliary tract disease (Q55785521) 3
Yes cytopenia (Q246147) 3
Yes cancer (Q12078) 3
Yes arteriosclerosis (Q184559) 3
Yes rare genetic renal disease (Q55789069) 3
Yes syndrome with 46,XY disorder of sex development (Q55789077) 3
Yes conjunctival disease (Q18556249) 3
Yes total autosomal trisomy (Q55789082) 3
Yes malformation syndrome with odontal and/or periodontal component (Q55785406) 3
Yes genetic lipodystrophy (Q55789109) 3
Yes branchial arch or oral-acral syndrome (Q55785404) 3
Yes Ascaridida infectious disease (Q18975942) 3
Yes deformity of chest and rib (Q25377767) 3
Yes ocular motility disease (Q11583708) 3
Yes idiopathic inflammatory myopathy (Q55789135) 3
Yes thiamine deficiency (Q4138763) 3
Yes neutropenia (Q1435822) 3
Yes focal dystonia (Q1428695) 3
Yes sulfuraminoacidemia (Q19001322) 3
Yes subcutaneous tissue disease (Q55788601) 3
Yes mixed dermis disorder (Q55788599) 3
Yes multiple endocrine neoplasia (Q1553018) 3
Yes dermis elastic tissue disorder (Q55788598) 3
Yes primary orthostatic hypotension (Q55785810) 3
Yes dichromatopsia (Q905389) 3
Yes RASopathy (Q1029344) 3
Yes dystonia (Q906492) 3
Yes idiopathic interstitial pneumonia (Q1790424) 3
Yes hyperpigmentation of the skin (Q55788594) 3
Yes prostate disease (Q18556445) 3
Yes arenavirus hemorrhagic fever (Q19001357) 3
Yes inflammatory bowel diseases (Q917447) 3
Yes inherited skin tumor (Q55785837) 3
Yes genetic photodermatosis (Q55785838) 3
Yes peripheral artery disease (Q378681) 3
Yes allergic contact dermatitis (Q12077704) 3
Yes cerebral malformation with epilepsy (Q55785630) 3
Yes shock (Q178061) 3
Yes thalamic disease (Q18556419) 3
Yes chlamydia infection (Q153356) 3
Yes pancreatitis (Q1527888) 3
Yes joint dislocation (Q324509) 2
Yes physical urticaria (Q7189630) 2
Yes genetic deafness (Q3505181) 2
Yes parathyroid neoplasm (Q7136148) 2
Yes abdominal hernia (Q3134277) 2
Yes bladder exstrophy-epispadias-cloacal exstrophy complex (Q32137168) 2
Yes atrial tachycardia (Q3513641) 2
Yes candidiasis (Q273510) 2
Yes penetrating trauma (Q7162621) 2
Yes elimination disorders (Q69906769) 2
Yes glomerulopathy (Q3347169) 2
Yes delusional disorder (Q721073) 2
Yes deficiency anemia (Q7070519) 2
Yes infectious arthropathy (Q70971408) 2
Yes birthmark (Q3513591) 2
Yes paraneoplastic neurologic syndrome (Q3508804) 2
Yes neuromuscular junction disease (Q7002430) 2
Yes hypobetalipoproteinemia (Q3444851) 2
Yes congenital vertebral anomaly (Q332343) 2
Yes leishmaniasis (Q331283) 2
Yes Primary lymphedema (Q7243149) 2
Yes nephrosis (Q6995207) 2
Yes seafood poisoning (Q3147703) 2
Yes neonatal alloimmune disease (Q3149939) 2
Yes multiple carboxylase deficiency (Q6934914) 2
Yes oral-facial-digital syndrome (Q3508783) 2
Yes multiple abnormalities (Q6934911) 2
Yes breast neoplasm (Q23929670) 2
Yes peritonitis (Q223102) 2
Yes tremor (Q223907) 2
Yes neuromuscular disease (Q2246789) 2
Yes cortical hyperostosis (Q9292374) 2
Yes osteophyte (Q923339) 2
Yes sensory loss (Q2289481) 2
Yes primordial dwarfism (Q2289761) 2
Yes hypopituitarism (Q922411) 2
Yes tetrasomy (Q906664) 2
Yes internal bleeding (Q2361887) 2
Yes amelia (Q23900578) 2
Yes urinary tract infection (Q221668) 2
Yes effusion (Q2398806) 2
Yes learning disability (Q860740) 2
Yes hyperthermia (Q242165) 2
Yes immunoproliferative disorder (Q8578535) 2
Yes trypanosomiasis (Q2443552) 2
Yes convulsion (Q852376) 2
Yes cystitis (Q246084) 2
Yes lichen planus (Q848371) 2
Yes tumor of hematopoietic and lymphoid tissues (Q2509220) 2
Yes diverticular disease (Q25324086) 2
Yes neurofibromatoses (Q847605) 2
No heart sound (Q967103) 2
Yes adverse effect (Q2047938) 2
Yes abnormal breathing (Q2056816) 2
Yes endometriosis (Q205764) 2
Yes pollution related disease (Q995620) 2
Yes microscopic colitis (Q2058941) 2
Yes pre-excitation syndrome (Q2064167) 2
Yes macrocytic anemia (Q2070695) 2
Yes eczema (Q988594) 2
Yes congenital bone marrow failure syndromes (Q98713408) 2
Yes Fusobacterium infections (Q98456483) 2
Yes acute leukemia (Q976388) 2
Yes aspergillosis (Q259626) 2
Yes chromosomal duplication syndrome (Q21082526) 2
Yes skin necrosis (Q21117421) 2
Yes Cold autoimmune hemolytic anemia (Q9615018) 2
Yes diaphragmatic hernia (Q2119430) 2
Yes scleroderma (Q958797) 2
Yes synostosis (Q2141048) 2
Yes red–green color blindness (Q2167988) 2
Yes bradycardia (Q217111) 2
Yes myelodysplastic syndrome (Q954625) 2
Yes radiologic sign (Q2202754) 2
Yes shoulder problem (Q7502714) 2
Yes abdominal wall defect (Q2852251) 2
Yes autoimmune hemolytic anemia (Q28814) 2
Yes impetigo (Q28971) 2
Yes T cell deficiency (Q7672692) 2
Yes alcohol withdrawal syndrome (Q2914873) 2
Yes T-cell lymphoma (Q7667896) 2
Yes atrial heart septal defect (Q757749) 2
Yes photosensitivity (Q2944236) 2
Yes leukemia (Q29496) 2
Yes spinal curvature (Q7577456) 2
Yes facial paralysis (Q7562539) 2
Yes intra-abdominal abscess (Q28501458) 2
Yes short stature (Q7502090) 2
Yes chromosome abnormality (Q744962) 2
Yes tapeworm infection (Q7356544) 2
Yes respiratory system cancer (Q7315926) 2
Yes undernutrition (Q3044538) 2
Yes hemiplegia (Q304497) 2
Yes envenomation (Q3055418) 2
Yes emotional and behavioral disorders (Q3063847) 2
Yes progressive myoclonus epilepsy (Q7248853) 2
Yes developmental disorder (Q3087172) 2
Yes women's health (Q8031191) 2
Yes blepharitis (Q845698) 2
Yes thrombosis (Q261327) 2
Yes diffuse large B-cell lymphoma (Q2626074) 2
Yes epulis (Q841989) 2
Yes endocrine system disease (Q2661443) 2
Yes multiple sclerosis (Q8277) 2
Yes congenital color blindness (Q26738259) 2
Yes factitious disorder (Q2686385) 2
Yes endocarditis (Q82504) 2
Yes personality disorder (Q270673) 2
Yes pseudohypoparathyroidism (Q819207) 2
Yes epidermolysis bullosa simplex (Q3124960) 2
Yes thrombocytopenic purpura (Q6132707) 2
Yes cutis laxa (Q2735907) 2
Yes macular degeneration (Q27429789) 2
Yes acne (Q79928) 2
Yes Tuberculid (Q7850836) 2
Yes rat-bite fever (Q2754970) 2
Yes uveitis (Q280027) 2
Yes dilated cardiomyopathy (Q283656) 2
Yes influenza (Q2840) 2
Yes ehrlichiosis (Q2845432) 2
Yes neurocutaneous syndrome with epilepsy (Q55785626) 2
Yes predominantly medium-vessel vasculitis (Q55785505) 2
Yes nose and cavum anomaly (Q55785515) 2
Yes rare allergic respiratory disease (Q55789066) 2
Yes rare disease with odontological manifestation (Q55789054) 2
Yes acquired pituitary hormone deficiency (Q55788906) 2
Yes hematological disorder with renal involvement (Q55788858) 2
Yes genetic hematologic disease (Q55785542) 2
Yes basal epidermolysis bullosa simplex (Q55785544) 2
Yes rare genetic gastroenterological disease (Q55785595) 2
Yes rare genetic intestinal disease (Q55785596) 2
Yes genetic pancreatic disease (Q55785598) 2
Yes syndromic urogenital tract malformation (Q55785600) 2
Yes primary bone dysplasia with disorganized development of skeletal components (Q55788820) 2
Yes rare head and neck malformation (Q55785495) 2
Yes bent bone dysplasia (Q55788810) 2
Yes type 11 collagen-related bone disorder (Q55788799) 2
Yes immune deficiency with skin involvement (Q55788607) 2
Yes DNA repair defect other than combined T-cell and B-cell immunodeficiencies (Q55785655) 2
Yes rare neuroinflammatory disease (Q55785812) 2
Yes syndromic neurometabolic disease with non-X-linked intellectual disability (Q55785813) 2
Yes dermis disorder (Q55788597) 2
Yes non-syndromic urogenital tract malformation of male (Q55785825) 2
Yes sebaceous gland anomaly (Q55788592) 2
Yes hereditary ataxia (Q3731293) 2
Yes inherited epidermolysis bullosa (Q55788582) 2
Yes other metabolic disease with skin involvement (Q55788569) 2
Yes EEC syndrome and related syndrome (Q55789198) 2
Yes severe cutaneous adverse reactions (Q55632923) 2
Yes varicella zoster infection (Q55779917) 2
Yes myopathy with eye involvement (Q55789252) 2
Yes non-neoplastic bile duct disorder (Q55780106) 2
Yes nose, anomalous shape of (Q55781290) 2
Yes hereditary optic neuropathy (Q55789244) 2
Yes congenital vitreoretinal dysplasia (Q55789243) 2
Yes rare parenchymal liver disease (Q55785260) 2
Yes craniofacial anomaly with cataract (Q55789231) 2
Yes cataract associated with a metabolic disease (Q55789224) 2
Yes unexplained periodic fever syndrome (Q55785287) 2
Yes chromosomal anomaly with cataract (Q55789222) 2
Yes syndromic myopia (Q55789206) 2
Yes inborn disorder of ornithine or proline metabolism (Q55788551) 2
Yes arthrogryposis multiplex congenita (Q55785297) 2
Yes eyebrow/eyelashes pigmentation anomaly (Q55789194) 2
Yes congenital intestinal transport defect (Q55785305) 2
Yes syndromic ankyloblepharon (Q55789160) 2
Yes microblepharon-ablephara syndrome (Q55789158) 2
Yes rare eye disease due to a differentiation anomaly (Q55789154) 2
Yes syndromic aniridia (Q55789153) 2
Yes teratogenic Pierre robin syndrome (Q55785395) 2
Yes constitutional hemolytic anemia due to acanthocytosis (Q55789124) 2
Yes hereditary haemolytic anaemia due to red cell membrane defects (Q55789123) 2
Yes rare developmental defect with connective tissue involvement (Q55785403) 2
Yes constitutional anemia due to iron metabolism disorder (Q55789120) 2
Yes disorder of carnitine cycle and carnitine transport (Q55787303) 2
Yes malformation of the neurenteric canal, spinal cord and column (Q55786799) 2
Yes Encephaloclastic disorder (Q55786814) 2
Yes rare hemorrhagic disorder due to a qualitative platelet defect (Q55786859) 2
Yes systemic diseases with panuveitis (Q55786946) 2
Yes rare disease with thoracic aortic aneurysm and aortic dissection (Q55786976) 2
Yes Epstein-Barr virus-associated malignant lymphoproliferative disorder (Q55786997) 2
Yes disorder of lysine and hydroxylysine metabolism (Q55787002) 2
Yes rare capillary malformation with associated anomalies (Q55788279) 2
Yes pseudohypoparathyroidism with Albright hereditary osteodystrophy (Q55788263) 2
Yes rare disease with myoclonus as a major feature (Q55787252) 2
Yes autosomal dominant diffuse mutilating palmoplantar keratoderma (Q55787267) 2
Yes disorder of neutral amino acid transport (Q55787282) 2
Yes disorder of fatty acid oxidation and ketogenesis (Q55787301) 2
Yes complex chromosomal rearrangement (Q55786712) 2
Yes disorder of zinc metabolism (Q55787339) 2
Yes disease with Cushing syndrome as a major feature (Q55787417) 2
Yes granulomatous autoinflammatory syndrome (Q55787619) 2
Yes fetal lower urinary tract obstruction (Q55788175) 2
Yes eosinophilic gastrointestinal disease (Q55788085) 2
Yes other immunodeficiency syndromes due to defects in innate immunity (Q55787696) 2
Yes primary bone dysplasia (Q55787804) 2
Yes primary bone dysplasia with progressive ossification of skin, skeletal muscle, fascia, tendons and ligaments (Q55787806) 2
Yes primary bone dysplasia with micromelia (Q55787807) 2
Yes sphingolipidosis with epilepsy (Q55787921) 2
Yes rare male infertility due to testicular endocrine disorder (Q55788025) 2
Yes rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin (Q55788062) 2
Yes non-familial dilated cardiomyopathy (Q55786154) 2
Yes inherited syndrome with bone tumors as a major feature (Q55785845) 2
Yes cerebral organic aciduria (Q55788538) 2
Yes inherited renal tubular disease (Q55785848) 2
Yes intractable diarrhea of infancy (Q55788495) 2
Yes hereditary eye tumor (Q55785853) 2
Yes rare genetic diabetes mellitus (Q55785854) 2
Yes progressive muscular dystrophy (Q55785935) 2
Yes non-dystrophic myopathy (Q55785938) 2
Yes autoimmune thrombocytopenia (Q55788483) 2
Yes complex vascular malformation with associated anomalies (Q55786077) 2
Yes hereditary thrombophilia (Q55786139) 2
Yes syndrome with brachydactyly (Q55788468) 2
Yes gingival disease (Q5563106) 2
Yes rare maxillo-facial surgical disease (Q55788454) 2
Yes familial restrictive cardiomyopathy (Q55786155) 2
Yes lysosomal disease with restrictive cardiomyopathy (Q55786156) 2
Yes hereditary poikiloderma (Q55786182) 2
Yes metal transport or utilization disorder with epilepsy (Q55786195) 2
Yes Moyamoya syndrome (Q55788342) 2
Yes genetic vascular disease (Q55786280) 2
Yes immune-mediated acquired neuromuscular junction disease (Q55788305) 2
Yes primary lymphedema with associated anomalies (Q55788282) 2
Yes partial deletion of the short arm of chromosome 11 (Q55786596) 2
Yes Duchenne and Becker muscular dystrophy (Q55786602) 2
Yes partial deletion of the long arm of chromosome 22 (Q55786629) 2
Yes adrenal gland hyperfunction (Q4684750) 2
Yes autoimmune polyendocrine syndrome (Q675311) 2
Yes Mannosidosis (Q6750947) 2
Yes ankylosis (Q418418) 2
Yes hypervitaminosis (Q423927) 2
Yes intracranial hemorrhage (Q426199) 2
Yes pharyngeal diseases (Q66793652) 2
Yes mental depression (Q4340209) 2
Yes herpangina (Q665258) 2
Yes withdrawal symptom (Q4420149) 2
Yes cold injury (Q4499376) 2
Yes metabolic syndrome (Q657193) 2
Yes acrodermatitis (Q4675757) 2
Yes acropustulosis (Q4676432) 2
Yes schizophrenia (Q41112) 2
Yes hip dysplasia (Q625935) 2
Yes newborn respiratory distress syndrome (Q47519106) 2
Yes intestinal parasite infection (Q475510) 2
Yes anorectal disorder (Q4770164) 2
Yes asbestos-related disease (Q4803677) 2
Yes dysphagia (Q623289) 2
Yes aortic aneurysm (Q616003) 2
Yes autosomal recessive cerebellar ataxia (Q4826996) 2
Yes brain ischemia (Q4862390) 2
Yes torticollis (Q615363) 2
Yes body-focused repetitive behavior disorders (Q4936774) 2
Yes neck injury (Q6152017) 2
Yes melanocytic nevus (Q377568) 2
Yes adenocarcinoma (Q356033) 2
Yes epidermolysis bullosa dystrophica (Q3589131) 2
Yes erythroblastopenia (Q3591490) 2
Yes Corynebacterium infection (Q69084244) 2
Yes intrahepatic cholestasis (Q3682587) 2
Yes leprosy (Q36956) 2
Yes hereditary sensory and autonomic neuropathy (Q3702898) 2
Yes mitochondrial myopathy (Q6881881) 2
Yes dermatoheliosis (Q3705873) 2
Yes dyskeratosis congenita (Q3709312) 2
Yes mitochondrial encephalomyopathy (Q6881866) 2
Yes minor physical anomaly (Q6869195) 2
Yes environmental disease (Q3751709) 2
Yes tendinitis (Q499574) 2
Yes granulocytosis (Q3775781) 2
Yes bacterial pneumonia (Q3776920) 2
Yes metabolic bone disease (Q6822340) 2
Yes labyrinthosis (Q3825166) 2
Yes palsy (Q68212673) 2
Yes poisoning by drugs (Q387175) 2
Yes hazardous chemical exposure (Q68182219) 2
Yes Erythropoietic porphyria (Q3908491) 2
Yes nephritis (Q401402) 2
Yes marfanoid (Q6759035) 2
Yes mercury poisoning (Q408089) 2
Yes protein-energy malnutrition (Q4082071) 2
Yes arm injuries (Q55040509) 2
Yes angiitis (Q539392) 2
Yes Erythrokeratodermia (Q5396475) 2
Yes hereditary optic atrophy (Q54087187) 2
Too many results. 1897 items skipped

"Unique value" violations[edit]

Violations count: 311

"Format" violations[edit]

Violations count: 14

"Scope" violations[edit]

Violations count: 0

"Entity types" violations[edit]

Violations count: 0

Retrieved from "https://www.wikidata.org/w/index.php?title=Wikidata:Database_reports/Constraint_violations/P557&oldid=2146704883"