Wolf-Hirschhorn syndrome English (Q610075)

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chromosome abnormality with a distinct craniofacial phenotype and intellectual disability English
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Language Label Description Also known as
English
Wolf-Hirschhorn syndrome
chromosome abnormality with a distinct craniofacial phenotype and intellectual disability
  • 4p deletion syndrome
  • chromosome deletion Dillan 4p syndrome
  • Pitt syndrome
  • Pitt–Rogers–Danks syndrome
  • WHS
  • PRDS
  • Pitt-Rogers-Danks Syndrome
  • chromosome 4p16.3 deletion syndrome
  • Wolf–Hirschhorn syndrome
  • Dillan 4p syndrome
  • 4p-syndrome

Statements

instance of English
class of disease English
0 references
subclass of English
chromosomal deletion syndrome English
1 reference
stated in English
Disease Ontology English
retrieved English
29 November 2020
Disease Ontology ID English
DOID:0050460
disease English
0 references
image English
Mia - whs.jpg
1,360 × 2,048; 295 KB
0 references
named after English
Kurt Hirschhorn English
0 references
Ulrich Wolf English
0 references
health specialty English
medical genetics English
0 references
NCI Thesaurus ID English
C35528
1 reference
stated in English
Disease Ontology English
retrieved English
28 August 2019
Disease Ontology ID English
DOID:0050460
Commons category English
Wolf–Hirschhorn syndrome
0 references

Identifiers

MeSH descriptor ID English
D054877
1 reference
stated in English
Disease Ontology English
retrieved English
28 August 2019
Disease Ontology ID English
DOID:0050460
MeSH tree code English
C16.131.077.944
0 references
C16.131.260.985
0 references
C16.320.180.985
0 references
KEGG ID English
H01773
0 references
DeCS ID English
52626
0 references
Disease Ontology ID English
DOID:0050460
1 reference
stated in English
Disease Ontology English
retrieved English
29 November 2020
Disease Ontology ID English
DOID:0050460
DiseasesDB English
eMedicine ID English
Freebase ID English
/m/0467g2
1 reference
stated in English
Freebase Data Dumps English
publication date English
28 October 2013
GARD rare disease ID English
7896
1 reference
stated in English
Disease Ontology English
retrieved English
28 August 2019
Disease Ontology ID English
DOID:0050460
GSSO ID English
006998
0 references
ICD-10-CM English
Q93.3
1 reference
stated in English
Disease Ontology English
retrieved English
28 August 2019
Disease Ontology ID English
DOID:0050460
ICD-11 ID (Foundation) English
1337401724
0 references
ICD-9 ID English
Microsoft Academic ID English
2909089631
0 references
2780192111
0 references
OMIM ID English
194190
1 reference
stated in English
Disease Ontology English
retrieved English
28 August 2019
Disease Ontology ID English
DOID:0050460
Orphanet ID English
280
1 reference
stated in English
Disease Ontology English
retrieved English
28 August 2019
Disease Ontology ID English
DOID:0050460
UMLS CUI English
C0796117
1 reference
stated in English
Disease Ontology English
retrieved English
28 August 2019
Disease Ontology ID English
DOID:0050460
C1956097
1 reference
stated in English
Disease Ontology English
retrieved English
28 August 2019
Disease Ontology ID English
DOID:0050460
 
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