Details of Disease | DrugMAP

General Information of Disease (ID: DISYR1KX)

Disease Name	Intellectual disability, autosomal dominant 53
Synonyms	MRD53; autosomal dominant mental retardation 53; mental retardation, autosomal dominant 53; autosomal dominant intellectual disability 53; intellectual disability, autosomal dominant 53
Disease Hierarchy	DISD6L06: Autosomal dominant non-syndromic intellectual disability DISYR1KX: Intellectual disability, autosomal dominant 53
Disease Identifiers	MONDO ID MONDO_0030919 UMLS CUI C4540481 OMIM ID 617798 MedGen ID 1623344

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
CAMK2A	OTJGX19T	Strong	Autosomal dominant	[1]
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References

1	Impaired spatial learning in alpha-calcium-calmodulin kinase II mutant mice. Science. 1992 Jul 10;257(5067):206-11. doi: 10.1126/science.1321493.