Details of Disease | DrugMAP

General Information of Disease (ID: DISA0LAP)

Disease Name	Intellectual disability, X-linked 101
Synonyms	MRX101; mental retardation, X-linked 101; intellectual disability, X-linked type 101; MID2 non-syndromic X-linked intellectual disability; mental retardation, X-linked type 101; intellectual developmental disorder, X-linked 101, X-linked recessive; intellectual disability, X-linked 101; non-syndromic X-linked intellectual disability caused by mutation in MID2
Definition	Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the MID2 gene.
Disease Hierarchy	DIS71AI3: Non-syndromic X-linked intellectual disability DISA0LAP: Intellectual disability, X-linked 101
Disease Identifiers	MONDO ID MONDO_0010489 UMLS CUI C3890168 OMIM ID 300928 MedGen ID 855517

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
MID2	OTAAQNZA	Limited	Unknown	[1]
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References

1	Targeted deep resequencing identifies MID2 mutation for X-linked intellectual disability with varied disease severity in a large kindred from India. Hum Mutat. 2014 Jan;35(1):41-4. doi: 10.1002/humu.22453. Epub 2013 Oct 21.