Autophagic vacuoles
Symptom Information:
Symptom ID: | HPO:0003736 | ||
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) Autophagic vacuoles(HPO:0003736) MedDRA: |
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Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Alpha-crystallinopathy | (Orphanet:98910) |
Autosomal dominant limb-girdle muscular dystrophy type 1F | (Orphanet:55595) |
Glycogen storage disease due to LAMP-2 deficiency | (Orphanet:34587) |
MYOPATHY, AUTOPHAGIC VACUOLAR, INFANTILE-ONSET | (OMIM:609500) |
ZASP-related myofibrillar myopathy | (Orphanet:98912) |