Details of Disease | DrugMAP

General Information of Disease (ID: DISQ36PG)

Disease Name	Neurooculocardiogenitourinary syndrome
Synonyms	NEUROOCULOCARDIOGENITOURINARY SYNDROME; NOCGUS
Disease Hierarchy	DISYKSRF: Genetic disease DISQ36PG: Neurooculocardiogenitourinary syndrome
Disease Identifiers	MONDO ID MONDO_0032850 UMLS CUI C5231443 OMIM ID 618652 MedGen ID 1684841

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
WDR37	OTOZUONG	Definitive	Autosomal dominant	[1]
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References

1	The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources. Genet Med. 2022 Aug;24(8):1732-1742. doi: 10.1016/j.gim.2022.04.017. Epub 2022 May 4.