| Term Name: | neurooculocardiogenitourinary syndrome |
|---|---|
| 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. |
| Ontology: | Human Disease [DOID:0111675] ( DOID:0111675 ) |