Details of Disease | DrugMAP

General Information of Disease (ID: DISDUY6J)

Disease Name	Intellectual developmental disorder, autosomal recessive 78
Disease Hierarchy	DISJWRZZ: Autosomal recessive non-syndromic intellectual disability DISDUY6J: Intellectual developmental disorder, autosomal recessive 78
Disease Identifiers	MONDO ID MONDO_0859373 UMLS CUI C5830269 OMIM ID 620237 MedGen ID 1840905

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
WDR11	OT5CY5UR	Strong	Autosomal recessive	[1]
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References

1	Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability. Eur J Hum Genet. 2021 Nov;29(11):1663-1668. doi: 10.1038/s41431-021-00943-5. Epub 2021 Aug 20.