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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	MIM:618652
Synonyms	NOCGUS [EXACT]
Parent Relationships	is_a autosomal dominant disease is_a syndrome
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance