Details of Disease | DrugMAP

General Information of Disease (ID: DISDH7FP)

Disease Name	Obsolete Duchenne and Becker muscular dystrophy
Synonyms	severe dystrophinopathy, Duchenne and Becker type
Definition	OBSOLETE. Duchenne and Becker muscular dystrophies (DMD and BMD) are neuromuscular diseases characterized by progressive muscle wasting and weakness due to degeneration of skeletal, smooth and cardiac muscle.
Disease Hierarchy	DIS01GPL: Grass pollen hypersensitivity DISDH7FP: Obsolete Duchenne and Becker muscular dystrophy

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.