Details of Disease | DrugMAP

General Information of Disease (ID: DIS1S9G0)

Disease Name	Galloway-Mowat syndrome 4
Synonyms	GAMOS4; Galloway-Mowat syndrome 4
Disease Hierarchy	DISVB7IM: Galloway-Mowat syndrome DIS1S9G0: Galloway-Mowat syndrome 4
Disease Identifiers	MONDO ID MONDO_0033008 UMLS CUI C4540270 OMIM ID 617730 MedGen ID 1613511

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
TP53RK	OTARRZAB	Strong	Autosomal recessive	[1]
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References

1	Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly. Nat Genet. 2017 Oct;49(10):1529-1538. doi: 10.1038/ng.3933. Epub 2017 Aug 14.