ZFIN Human Disease: neurooculocardiogenitourinary syndrome

OBO ID: DOID:0111675

Term Name:	neurooculocardiogenitourinary syndrome		Search Ontology:
Synonyms:	NOCGUS
Definition:	A syndrome characterized by impaired growth and anomalies of the ocular, craniofacial, neurologic, cardiovascular, genitourinary, skeletal, and gastrointestinal systems that has_material_basis_in heterozygous mutation in the WDR37 gene on chromosome 10p15.3. https://www.ncbi.nlm.nih.gov/pubmed/31327510
References:	OMIM:618652
Ontology:	Human Disease ( DOID:0111675 )

Relationships

is a type of:	autosomal dominant disease syndrome autosomal dominant disease syndrome Show first 5 Terms

OTHER neurooculocardiogenitourinary syndrome PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
WDR37	wdr37	Neurooculocardiogenitourinary syndrome	618652

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None