Sternocleidomastoid amyotrophy
Symptom Information:
| Symptom ID: | HPO:0012036 | ||
| Synonyms: |
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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) Sternocleidomastoid amyotrophy(HPO:0012036) MedDRA: |
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| Database Frequency: | 2 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Congenital muscular dystrophy type 1B | (Orphanet:98893) |
| Steinert myotonic dystrophy | (Orphanet:273) |