Details of Disease | DrugMAP

General Information of Disease (ID: DISW401P)

Disease Name	Intellectual developmental disorder, autosomal dominant 65
Synonyms	mental retardation, autosomal dominant 65; MRD65
Disease Hierarchy	DIS1I87P: Intellectual disability, autosomal dominant DISW401P: Intellectual developmental disorder, autosomal dominant 65
Disease Identifiers	MONDO ID MONDO_0023657 UMLS CUI C5543371 OMIM ID 619320 MedGen ID 1787923

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
KDM4B	OT5P1UPY	Strong	Autosomal dominant	[1]
------------------------------------------------------------------------------------

References

1	CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens. Sci Rep. 2016 Jun 3;6:25954. doi: 10.1038/srep25954.