Pectoralis amyotrophy
Symptom Information:
| Symptom ID: | HPO:0012037 | ||||
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| Is a (Direct Parents): |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) Abnormality of the musculature of the thorax(HPO:0009131) Abnormality of the pectoral muscle(HPO:0011957) Pectoralis amyotrophy(HPO:0012037) Abnormality of muscle morphology(HPO:0011805) Skeletal muscle atrophy(HPO:0003202) Pectoralis amyotrophy(HPO:0012037) MedDRA: |
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| Database Frequency: | 1 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Congenital muscular dystrophy type 1B | (Orphanet:98893) |