Human genes for neurooculocardiogenitourinary syndrome
Neurooculocardiogenitourinary syndrome [DOID:0111675]
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 WDR37 on chromosome 10p15.3.
Synonyms: neurooculocardiogenitourinary syndrome, DOID:0111675, neurooculocardiogenitourinary disease, neurooculocardiogenitourinary disorder, neurooculocardiogenitourinary syndromes ...