Details of Disease | DrugMAP

General Information of Disease (ID: DIS1GSMA)

Disease Name	Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development
Synonyms	PNRIID; peripheral neuropathy, autosomal recessive, with or without impaired intellectual development
Disease Hierarchy	DISYKSRF: Genetic disease DIS1GSMA: Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development
Disease Identifiers	MONDO ID MONDO_0029131 UMLS CUI C4748283 OMIM ID 618124 MedGen ID 1648480

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
MCM3AP	OT895FEC	Definitive	Autosomal recessive	[1]
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References

1	Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen). Genet Med. 2020 Feb;22(2):245-257. doi: 10.1038/s41436-019-0686-8. Epub 2019 Nov 6.