Muscle fiber atrophy
Symptom Information:
Symptom ID: | HPO:0100295 | ||||||||||||||||||||||||||
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) Muscle fiber atrophy(HPO:0100295) MedDRA: Nervous system disorders(MedDRA:10029205) Neuromuscular disorders(MedDRA:10029317) Neuromuscular disorders NEC(MedDRA:10029318) Muscle fiber atrophy(HPO:0100295) |
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Database Frequency: | 22 / 7739 | ||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
Autosomal recessive limb-girdle muscular dystrophy type 2C | (Orphanet:353) |
Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
CANDLE syndrome | (Orphanet:325004) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Carney complex | (Orphanet:1359) |
Cushing disease | (Orphanet:96253) |
Frontometaphyseal dysplasia | (Orphanet:1826) |
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 2 | (OMIM:615422) |
JMP syndrome | (Orphanet:324999) |
Kearns-Sayre syndrome | (Orphanet:480) |
Leprechaunism | (Orphanet:508) |
MELAS | (Orphanet:550) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE) | (OMIM:615418) |
Mitochondrial DNA deletion syndrome with progressive myopathy | (Orphanet:352470) |
Mitochondrial myopathy and sideroblastic anemia | (Orphanet:2598) |
Myopathy, lactic acidosis, and sideroblastic anemia 2; MLASA2 | (OMIM:613561) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Proteasome disability syndrome | (Orphanet:324977) |
Sialidosis type 1 | (Orphanet:812) |
Steinert myotonic dystrophy | (Orphanet:273) |
Werner syndrome | (Orphanet:902) |