OMOP Concept 37395782

Autosomal recessive limb girdle muscular dystrophy type 2A

StandardConditionSNOMED715341003Disorder
Maps from
3
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
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Source codes that map to this concept

3 source codes normalize to Autosomal recessive limb girdle muscular dystrophy type 2A via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for Autosomal recessive limb girdle muscular dystrophy type 2A across source vocabularies.

  • Autosomal recessive limb girdle muscular dystrophy type 2A (disorder)
  • Calpain-3 deficiency limb girdle muscular dystrophy type 2A
  • distrofia muscular de las cinturas de las extremidades tipo 2A autosómica recesiva
  • distrofia muscular de las cinturas de las extremidades tipo 2A autosómica recesiva (trastorno)
  • distrofia muscular de las cinturas de los miembros tipo 2A por deficiencia de calpaína 3
  • distrofia muscular de las cinturas escapular y pélvica tipo 2A autosómica recesiva
  • Leyden-Möbius muscular dystrophy
  • Primary calpainopathy

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

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