Generalized amyotrophy
Symptom Information:
Symptom ID: | HPO:0003700 | |||||||||||||||||||||||||||||||||||||||
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) Skeletal muscle atrophy(HPO:0003202) Generalized amyotrophy(HPO:0003700) MedDRA: Nervous system disorders(MedDRA:10029205) Neuromuscular disorders(MedDRA:10029317) Neuromuscular disorders NEC(MedDRA:10029318) Generalized amyotrophy(HPO:0003700) |
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Database Frequency: | 39 / 7739 | |||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
2-methylbutyryl-CoA dehydrogenase deficiency | (Orphanet:79157) |
Allan-Herndon-Dudley syndrome | (Orphanet:59) |
Alpha-N-acetylgalactosaminidase deficiency | (Orphanet:3137) |
Alpha-N-acetylgalactosaminidase deficiency type 1 | (Orphanet:79279) |
Alpha-N-acetylgalactosaminidase deficiency type 3 | (Orphanet:79281) |
Autosomal dominant spastic paraplegia type 9 | (Orphanet:100990) |
Autosomal recessive centronuclear myopathy | (Orphanet:169186) |
Autosomal recessive limb-girdle muscular dystrophy type 2C | (Orphanet:353) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
BROWN-VIALETTO-VAN LAERE SYNDROME 2 | (OMIM:614707) |
CANDLE syndrome | (Orphanet:325004) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Carney complex | (Orphanet:1359) |
Classic multiminicore myopathy | (Orphanet:324604) |
Congenital muscular dystrophy due to LMNA mutation | (Orphanet:157973) |
Congenital muscular dystrophy, Ullrich type | (Orphanet:75840) |
Cushing disease | (Orphanet:96253) |
Desmin-related myopathy with Mallory body-like inclusions | (Orphanet:84132) |
Fetal akinesia deformation sequence | (Orphanet:994) |
Frontometaphyseal dysplasia | (Orphanet:1826) |
Glycogen storage disease due to LAMP-2 deficiency | (Orphanet:34587) |
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 DNA depletion syndrome, myopathic form | (Orphanet:254875) |
Mitochondrial myopathy and sideroblastic anemia | (Orphanet:2598) |
Muscular dystrophy, Selcen type | (Orphanet:199340) |
Myopathy, lactic acidosis, and sideroblastic anemia 2; MLASA2 | (OMIM:613561) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
OPTICOACOUSTIC NERVE ATROPHY WITH DEMENTIA | (OMIM:311150) |
Progressive external ophthalmoplegia - myopathy - emaciation | (Orphanet:352447) |
Proteasome disability syndrome | (Orphanet:324977) |
Rigid spine syndrome | (Orphanet:97244) |
Sialidosis type 1 | (Orphanet:812) |
Steinert myotonic dystrophy | (Orphanet:273) |
Werner syndrome | (Orphanet:902) |