Type 2 muscle fiber atrophy
Symptom Information:
Symptom ID: | HPO:0003554 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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 2 muscle fiber atrophy(HPO:0003554) MedDRA: |
||
Database Frequency: | 14 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Combined oxidative phosphorylation defect type 13 | (Orphanet:319514) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Glycogen storage disease due to muscle and heart glycogen synthase deficiency | (Orphanet:137625) |
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome | (Orphanet:363694) |
MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL | (OMIM:601462) |
MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL | (OMIM:608930) |
MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL | (OMIM:605809) |
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:608931) |
Myasthenia gravis | (Orphanet:589) |
Perrault Syndrome 5 | (OMIM:616138) |
Presynaptic congenital myasthenic syndromes | (Orphanet:98914) |
Proximal myotonic myopathy | (Orphanet:606) |
Synaptic congenital myasthenic syndromes | (Orphanet:98915) |
Tubular aggregate myopathy | (Orphanet:2593) |