Search Ontology:
Human Disease

neurooculocardiogenitourinary syndrome

Term ID
DOID:0111675
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
Ontology
Human Disease   ( DOID:0111675 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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