Details of Disease | DrugMAP

General Information of Disease (ID: DISBBEUO)

Disease Name	Muscular dystrophy, limb-girdle, autosomal recessive 23
Synonyms	LGMDR23; laminin subunit alpha 2-related limb-girdle muscular dystrophy R23; muscular dystrophy, limb-girdle, autosomal recessive 23
Disease Hierarchy	DIS99VM0: LAMA2-related muscular dystrophy DISWPGLM: Autosomal recessive limb-girdle muscular dystrophy DISBBEUO: Muscular dystrophy, limb-girdle, autosomal recessive 23
Disease Identifiers	MONDO ID MONDO_0029136 UMLS CUI C4748327 OMIM ID 618138 MedGen ID 1648462 Orphanet ID 565837

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
LAMA2	OTFROQWE	Strong	Autosomal recessive	[1]
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References

1	LAMA2 Muscular Dystrophy. 2012 Jun 7 [updated 2020 Sep 17]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews(?) [Internet]. Seattle (WA): University of Washington, Seattle; 1993C2024.