Details of Disease | DrugMAP

General Information of Disease (ID: DISVBZQN)

Disease Name	Intellectual disability, autosomal recessive 66
Synonyms	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66; MRT66; intellectual developmental disorder, autosomal recessive 66
Disease Hierarchy	DISJWRZZ: Autosomal recessive non-syndromic intellectual disability DISVBZQN: Intellectual disability, autosomal recessive 66
Disease Identifiers	MONDO ID MONDO_0032605 UMLS CUI C4748732 OMIM ID 618221 MedGen ID 1648460

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
FERRY3	OTCA1IVG	Strong	Autosomal recessive	[1]
------------------------------------------------------------------------------------

References

1	Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families. Cell Rep. 2015 Jan 13;10(2):148-61. doi: 10.1016/j.celrep.2014.12.015. Epub 2014 Dec 31.