| Metadata | |
|---|---|
| ID | DOID:0111675 |
| Name | neurooculocardiogenitourinary syndrome |
| 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 |
| Xrefs | |
| Synonyms |
NOCGUS [EXACT] |
| Parent Relationships |
is_a syndrome |