Details of Disease | DrugMAP

General Information of Disease (ID: DISAJ58X)

Disease Name	Intellectual developmental disorder, autosomal dominant 66
Synonyms	MRD66; mental retardation, autosomal dominant 66; intellectual developmental disorder, autosomal dominant 66
Disease Hierarchy	DIS1I87P: Intellectual disability, autosomal dominant DISAJ58X: Intellectual developmental disorder, autosomal dominant 66
Disease Identifiers	MONDO ID MONDO_0030891 UMLS CUI C5677000 OMIM ID 619910 MedGen ID 1812470

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTP Molecule(s)

Gene Name	DTP ID	Evidence Level	Mode of Inheritance	REF
ATP2B1	DTJWQ1L	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
ATP2B1	OT5MXG9W	Strong	Autosomal dominant	[1]
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References

1	Targeted ablation of plasma membrane Ca2+-ATPase (PMCA) 1 and 4 indicates a major housekeeping function for PMCA1 and a critical role in hyperactivated sperm motility and male fertility for PMCA4. J Biol Chem. 2004 Aug 6;279(32):33742-50. doi: 10.1074/jbc.M404628200. Epub 2004 Jun 3.