Scapuloperoneal amyotrophy

Symptom Information:

Symptom ID: HPO:0003697
Synonyms:
Scapuloperoneal atrophy [HPO:0003697]
Scapuloperoneal atrophy [OMIM:Scapuloperoneal atrophy]
Quality:
Cross references:
OMIM: "Scapuloperoneal atrophy" [OMIM:Scapuloperoneal atrophy]
Is a (Direct Parents):
HPO         Skeletal muscle atrophy
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle morphology(HPO:0011805)
             Skeletal muscle atrophy(HPO:0003202)
                Scapuloperoneal amyotrophy(HPO:0003697)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive lower motor neuron disease with childhood onset (Orphanet:206580)
Hyaline body myopathy (Orphanet:53698)
MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE (OMIM:255160)
MYOPATHY, MYOSIN STORAGE (OMIM:608358)
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY (OMIM:181405)