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Items: 4

Select item 17279011.

Facioscapulohumeral muscular dystrophy 1

Facioscapulohumeral muscular dystrophy (FSHD) typically presents with weakness of the facial muscles, the stabilizers of the scapula, or the dorsiflexors of the foot. Severity is highly variable. Weakness is slowly progressive and approximately 20% of affected individuals eventually require a wheelchair. Life expectancy is not shortened. [from GeneReviews]

MedGen UID:: 1727901
•Concept ID:: C5399970
•: Disease or Syndrome

Select item 3204052.

Facioscapulohumeral muscular dystrophy 2

Facioscapulohumeral muscular dystrophy (FSHD) typically presents with weakness of the facial muscles, the stabilizers of the scapula, or the dorsiflexors of the foot. Severity is highly variable. Weakness is slowly progressive and approximately 20% of affected individuals eventually require a wheelchair. Life expectancy is not shortened. [from GeneReviews]

MedGen UID:: 320405
•Concept ID:: C1834671
•: Disease or Syndrome

Select item 3718463.

Myopathy with storage of glycoproteins and Glycosaminoglycans

MedGen UID:: 371846
•Concept ID:: C1834532
•: Disease or Syndrome

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 983734.

Scapulohumeral muscular dystrophy

MedGen UID:: 98373
•Concept ID:: C0410192
•: Disease or Syndrome

GTR
ClinVar
Genes
OMIM
GeneReviews

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"Scapulohumeral muscular dystrophy"[Clinical Features] OR 98373[u... (4)
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