Details of Disease | DrugMAP

General Information of Disease (ID: DISGWGJ9)

Disease Name	Cataract 50 with or without glaucoma
Disease Hierarchy	DISUD7SL: Cataract DISGWGJ9: Cataract 50 with or without glaucoma
Disease Identifiers	MONDO ID MONDO_0859382 UMLS CUI C5830299 OMIM ID 620253 MedGen ID 1840935

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
TRPM3	TTO3TD8	Strong	Autosomal dominant	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
TRPM3	OTE4CDOQ	Strong	Autosomal dominant	[1]
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References

1	Mutation of the melastatin-related cation channel, TRPM3, underlies inherited cataract and glaucoma. PLoS One. 2014 Aug 4;9(8):e104000. doi: 10.1371/journal.pone.0104000. eCollection 2014.