Wikidata:Database reports/Constraint violations/P1199

From Wikidata
Jump to navigation Jump to search
Constraint violations report for mode of inheritance (Discussion, uses, items, changes, related properties): manner in which a particular genetic trait or disorder is passed from one generation to the next
Data time stamp: (UTC) — Items processed: 84
The report is generated based on the settings on Property:P1199#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: 1

"Type phenotypic trait (Q1211967), disease (Q12136)" violations[edit]

Violations count: 1

Types statistics[edit]

Accepted Type Usage
Yes rare disease (Q929833) 33
Yes disease (Q12136) 28
Yes developmental defect during embryogenesis (Q55788864) 23
Yes genetic disease (Q200779) 14
Yes autosomal recessive disease (Q10267817) 11
Yes autosomal dominant disease (Q18553439) 9
Yes mucopolysaccharidosis (Q1479681) 7
Yes designated intractable/rare disease (Q42303753) 5
Yes porphyria (Q271759) 5
Yes head and neck disease (Q55789477) 4
Yes porphyria due to ALAD deficiency (Q419897) 4
Yes syndrome (Q179630) 4
Yes lysosomal storage disease with skeletal involvement (Q55788818) 4
Yes chromosomal deletion syndrome (Q16918398) 4
Yes pure or complex hereditary spastic paraplegia (Q55346012) 3
Yes X-linked recessive disease (Q55010090) 3
Yes blood coagulation disease (Q890200) 3
Yes coagulation factor deficiency (Q18971506) 3
Yes chromosomal duplication syndrome (Q21082526) 3
Yes genetic syndromic intellectual disability (Q55785866) 3
Yes Erythropoietic porphyria (Q3908491) 2
Yes eye degenerative disease (Q18558225) 2
Yes metabolic disease with corneal opacity (Q55789274) 2
Yes inherited blood coagulation disease (Q18555031) 2
Yes genetic nervous system disorder (Q55788492) 2
Yes organic brain syndrome (Q360341) 2
Yes skin disease (Q949302) 2
Yes developmental anomaly of metabolic origin (Q55785399) 2
Yes orofacial clefting syndrome (Q55785405) 2
Yes rare syndrome with cardiac malformations (Q55785518) 2
Yes rare genetic developmental defect during embryogenesis (Q55785846) 2
Yes autosomal genetic disease (Q18553442) 2
Yes X-linked disease (Q18553438) 2
Yes X-linked intellectual disability (Q8041560) 2
Yes hemophilia (Q134003) 2
Yes partial duplication of the long arm of chromosome 17 (Q55786693) 1
Yes partial duplication of the short arm of chromosome 16 (Q55786658) 1
Yes syndrome with a cerebellar malformation as major feature (Q55786833) 1
Yes syndrome with limb reduction defects (Q55787046) 1
Yes rare genetic tremor disorder (Q55787262) 1
Yes keratitis (Q757838) 1
Yes autosomal dominant diffuse mutilating palmoplantar keratoderma (Q55787267) 1
Yes mitochondrial disorder due to a defect in assembly or maturation of the respiratory chain complexes (Q55787305) 1
Yes other immunodeficiency syndromes due to defects in innate immunity (Q55787696) 1
Yes hyper-IgE syndrome (Q55787700) 1
Yes rare disorder with dystonia and other neurologic or systemic manifestation (Q55787834) 1
Yes palmoplantar keratosis (Q7128426) 1
Yes multiple abnormalities (Q6934911) 1
Yes partial duplication of the long arm of chromosome 1 (Q55786662) 1
Yes lysosomal storage disease (Q675010) 1
Yes partial deletion of the long arm of chromosome 17 (Q55786617) 1
Yes partial monosomy of the long arm of chromosome 10 (Q55786612) 1
Yes neurofibromatoses (Q847605) 1
Yes partial deletion of the long arm of chromosome 1 (Q55786603) 1
Yes Auricular hypertrichosis (Q9003892) 1
Yes liver disease (Q929737) 1
Yes metal transport or utilization disorder with epilepsy (Q55786195) 1
Yes syndrome associated with hypertrophic cardiomyopathy (Q55786146) 1
Yes lysosomal disease with hypertrophic cardiomyopathy (Q55786143) 1
Yes mitochondrial disease (Q935710) 1
Yes multiple congenital anomalies/dysmorphic syndrome without intellectual disability (Q55785290) 1
Yes rare genetic epilepsy (Q55785842) 1
Yes genetic photodermatosis (Q55785838) 1
Yes primary bone dysplasia with decreased bone density (Q55788815) 1
Yes metabolic disease with cataract (Q55789275) 1
Yes congenital vitreoretinal dysplasia (Q55789243) 1
Yes hypoparathyroidism, familial isolated (Q55950233) 1
Yes colobomatous and areolar dystrophy (Q55789239) 1
Yes hyaline body myopathy (Q56014213) 1
Yes syndromic cataract (Q55789221) 1
Yes rare constitutional hemolytic anemia due to an enzyme disorder (Q55789125) 1
Yes proximal spinal muscular atrophy (Q56014257) 1
Yes acute hepatic porphyria (Q55788880) 1
Yes nervous system malformations (Q584265) 1
Yes adrenal hyperplasia (Q5898303) 1
Yes nephropathy secondary to a storage or other metabolic disease (Q55788855) 1
Yes syndromic renal or urinary tract malformation (Q55788832) 1
Yes primary microcephaly (Q60195167) 1
Yes rare male infertility due to testicular endocrine disorder (Q55788025) 1
Yes primary bone dysplasia with increased bone density (Q55788814) 1
Yes 46,XY disorder of sex development due to testicular steroidogenesis defect (Q55788739) 1
Yes syndromic genetic deafness (Q55788734) 1
Yes polycystic kidney disease (Q60195313) 1
Yes immune deficiency with skin involvement (Q55788607) 1
Yes mucopolysaccharidosis with skin involvement (Q55788606) 1
Yes inherited epidermolysis bullosa (Q55788582) 1
Yes inborn disorder of energy metabolism (Q55788564) 1
Yes ptosis (Q622427) 1
Yes rare hemorrhagic disorder due to a constitutional coagulation factors defect (Q55788455) 1
Yes dysostosis of genetic origin with limb anomaly as a major feature (Q55788097) 1
Yes rare female infertility due to adrenal disorder of genetic origin (Q55788069) 1
Yes genodermatosis (Q666075) 1
Yes rare male infertility due to adrenal disorder of genetic origin (Q55788063) 1
Yes nerve deafness (Q18967037) 1
Yes neuro-cardio-facial-cutaneous syndromes (Q17074582) 1
Yes mitochondrial DNA depletion syndrome (Q17144217) 1
Yes neurodegeneration (Q1755122) 1
Yes inherited metabolic disorder (Q1758393) 1
Yes brachyolmia (Q18553406) 1
Yes hyperimmunoglobulin syndrome (Q18555244) 1
Yes external ear disease (Q18556075) 1
Yes congenital nystagmus (Q18558184) 1
Yes cerebral degeneration (Q1620193) 1
Yes copper metabolism disease (Q19001238) 1
Yes viral infectious disease (Q1928978) 1
Yes iron overload (Q2025687) 1
Yes chronic progressive external ophthalmoplegia (Q2026857) 1
Yes tremor (Q223907) 1
Yes Stickler syndrome (Q2288646) 1
Yes amelia (Q23900578) 1
Yes malformation syndrome (Q1401195) 1
Yes muscular dystrophy (Q1137767) 1
Yes Wolfram syndrome (Q1153641) 1
Yes dacryocystitis (Q1157761) 1
Yes deafness (Q12133) 1
Yes vascular disease (Q1266890) 1
Yes adrenogenital disease (Q13368382) 1
Yes neurometabolic disease (Q1337418) 1
Yes hypertrophic cardiomyopathy (Q1364270) 1
Yes tumor of hematopoietic and lymphoid tissues (Q2509220) 1
Yes aplasia cutis congenita (Q1424491) 1
Yes osteopoikilosis (Q1477777) 1
Yes steroid inherited metabolic disorder (Q15051314) 1
No sequence variant (Q15304597) 1
Yes autosomal dominant polycystic kidney disease (Q15443105) 1
Yes hypoparathyroidism (Q1586088) 1
Yes popliteal pterygium syndrome (Q1587881) 1
Yes syndromic developmental defect of the eye (Q55785336) 1
Yes sheep disease (Q53582403) 1
Yes hereditary peripheral neuropathy (Q55012611) 1
Yes GM2 gangliosidosis (Q5513691) 1
Yes Huntington disease and related disorders (Q55345637) 1
Yes genetic neurodegenerative disease with dementia (Q55346116) 1
Yes hereditary hypercarotenemia and vitamin A deficiency (Q55780407) 1
Yes rare metabolic liver disease (Q55785261) 1
Yes multiple congenital anomalies/dysmorphic syndrome-intellectual disability (Q55785288) 1
Yes distal muscular dystrophy (Q5282843) 1
Yes malformation syndrome with short stature (Q55785400) 1
Yes genetic hematologic disease (Q55785542) 1
Yes rare abdominal surgical disease (Q55785601) 1
Yes chromosomal anomaly with epilepsy as a major feature (Q55785627) 1
Yes DNA repair defect other than combined T-cell and B-cell immunodeficiencies (Q55785655) 1
Yes syndromic neurometabolic disease with X-linked intellectual disability (Q55785814) 1
Yes polymalformative genetic syndrome with increased risk of developing cancer (Q55785832) 1
Yes metal metabolism disorder (Q3281373) 1
Yes sideroblastic anaemia P (Q2610084) 1
Yes atopic dermatitis (Q268667) 1
Yes familial hypercholesterolemia (Q2711291) 1
Yes cutis laxa (Q2735907) 1
Yes activated protein C resistance (Q296104) 1
Yes photodermatosis (Q2986815) 1
Yes primary immunodeficiency disease (Q3043160) 1
Yes peroxisomal disease (Q3281322) 1
Yes inherited skin tumor (Q55785837) 1
Yes trinucleotide repeat disorder (Q356736) 1
Yes epidermolysis bullosa dystrophica (Q3589131) 1
Yes Hereditary sideroblastic anemia (Q3616631) 1
Yes lymphoproliferative disorders (Q4165484) 1
Yes 2-hydroxyglutaric aciduria (Q4596888) 1
Yes spondylocostal dysostosis (Q4821698) 1
Yes Chromosome 15q partial deletion (Q5113911) 1

"Value type mode of inheritance (Q1348351)" violations[edit]

Violations count: 0

Types statistics[edit]

Accepted Type Usage
Yes mode of inheritance (Q1348351) 85

"Scope" violations[edit]

Violations count: 1

Retrieved from "https://www.wikidata.org/w/index.php?title=Wikidata:Database_reports/Constraint_violations/P1199&oldid=1967166875"