Details of Disease | DrugMAP

General Information of Disease (ID: DISRHNIN)

Disease Name	Intellectual developmental disorder, autosomal dominant 68
Synonyms	MRD68; intellectual developmental disorder, autosomal dominant 68; mental retardation, autosomal dominant 68
Disease Hierarchy	DIS1I87P: Intellectual disability, autosomal dominant DISRHNIN: Intellectual developmental disorder, autosomal dominant 68
Disease Identifiers	MONDO ID MONDO_0030969 UMLS CUI C5677008 OMIM ID 619934 MedGen ID 1802176

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
KMT2B	OTMMAZQX	Limited	Unknown	[1]
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References

1	Exome sequencing identifies three novel candidate genes implicated in intellectual disability. PLoS One. 2014 Nov 18;9(11):e112687. doi: 10.1371/journal.pone.0112687. eCollection 2014.