Type 1 muscle fiber atrophy
Symptom Information:
Symptom ID: | HPO:0011807 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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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 muscle morphology(HPO:0011805) Abnormality of muscle fibers(HPO:0004303) Muscle fiber atrophy(HPO:0100295) Type 1 muscle fiber atrophy(HPO:0011807) MedDRA: |
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Database Frequency: | 2 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Combined oxidative phosphorylation defect type 8 | (Orphanet:319504) |
[DEL]EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED | (OMIM:310300) |