Details of Disease | DrugMAP

General Information of Disease (ID: DISV66YX)

Disease Name	Progressive muscular dystrophy
Synonyms	progressive muscular dystrophy
Disease Hierarchy	DIS4550J: Muscle wasting disease DISV66YX: Progressive muscular dystrophy
Disease Identifiers	MONDO ID MONDO_0016106 UMLS CUI C4551827 MedGen ID 1633060 Orphanet ID 206644 SNOMED CT ID 193225000

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
DMD	TT2TNRM	Definitive	X-linked	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
DMD	OTD21T5J	Definitive	X-linked	[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.