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Fingerprint body myopathy

MedGen UID:
337026
Concept ID:
C1844560
Disease or Syndrome
Synonyms: Fingerprint Body Myopathy
Modes of inheritance:
X-linked inheritance
MedGen UID:
66838
Concept ID:
C0241764
Genetic Function
Sources: HPO, OMIM
A mode of inheritance that is observed for traits related to a gene encoded on the X chromosome.
 
OMIM®: 305550
Orphanet: ORPHA97232

Clinical features

Muscular Diseases
MedGen UID:
10135
Concept ID:
C0026848
Disease or Syndrome
A disorder of muscle unrelated to impairment of innervation or neuromuscular junction.
Abnormality of metabolism/homeostasis
MedGen UID:
867398
Concept ID:
C4021768
Finding

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVFingerprint body myopathy
Follow this link to review classifications for Fingerprint body myopathy in Orphanet.

Recent clinical studies

Etiology

Curless RG, Payne CM, Brinner FM
Dev Med Child Neurol 1978 Dec;20(6):793-8. PMID: 729932

Prognosis

Curless RG, Payne CM, Brinner FM
Dev Med Child Neurol 1978 Dec;20(6):793-8. PMID: 729932

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