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Qualitative or quantitative defects of delta-sarcoglycan

MedGen UID:: 1826098
•Concept ID:: C5680806
•: Disease or Syndrome

Synonym:	Delta-sarcoglycanopathy

Monarch Initiative:	MONDO:0016144
Orphanet:	ORPHA207070

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVLimb-girdle muscular dystrophy
- CROGVAutosomal recessive limb-girdle muscular dystrophy
- CROGVMuscular dystrophy, limb-girdle, autosomal dominant

Abnormality of limbs
- Abnormality of the musculature of the limbs
  - Limb-girdle muscle atrophy
    - Limb-girdle muscular dystrophy
      - Autosomal recessive limb-girdle muscular dystrophy
        Sarcoglycanopathy
        Qualitative or quantitative defects of delta-sarcoglycan
        Autosomal recessive limb-girdle muscular dystrophy type 2F

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Qualitative or quantitative defects of delta-sarcoglycan

Term Hierarchy

Professional guidelines

PubMed

Recent clinical studies

Therapy

Prognosis

Clinical prediction guides

Recent systematic reviews

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