Abnormality of muscle fibers
Symptom Information:
Symptom ID: | HPO:0004303 | ||||||||
Synonyms: |
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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) MedDRA: |
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Database Frequency: | 2 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Greig cephalopolysyndactyly syndrome | (Orphanet:380) |
MUSCULAR HYPOPLASIA, CONGENITAL UNIVERSAL, OF KRABBE | (OMIM:159100) |