neurooculocardiogenitourinary syndrome (DOID:0111675)
Alliance: disease page
Synonyms: NOCGUS
Alt IDs: OMIM:618652
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.