Details of Disease | DrugMAP

General Information of Disease (ID: DISGE7DR)

Disease Name	Intellectual developmental disorder 62
Synonyms	Mental Retardation, Autosomal Dominant 62; INTELLECTUAL DEVELOPMENTAL DISORDER 62; MRD62
Disease Hierarchy	DISD6L06: Autosomal dominant non-syndromic intellectual disability DISGE7DR: Intellectual developmental disorder 62
Disease Identifiers	MONDO ID MONDO_0032919 UMLS CUI C5394083 OMIM ID 618793 MedGen ID 1712636

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
DLG4	TT9PB26	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
DLG4	OTD9E2LU	Strong	Autosomal dominant	[1]
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References

1	Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications. Hum Mutat. 2017 May;38(5):600-608. doi: 10.1002/humu.23183. Epub 2017 Feb 13.