Scapuloperoneal amyotrophy
Symptom Information:
Symptom ID: | HPO:0003697 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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) |