Type 2 muscle fiber atrophy

Symptom Information:

Symptom ID: HPO:0003554
Synonyms:
Type 2 fiber atrophy [HPO:0003554]
Type 2 fiber atrophy [OMIM:Type 2 fiber atrophy]
Quality:
Cross references:
OMIM: "Type 2 fiber atrophy" [OMIM:Type 2 fiber atrophy]
Is a (Direct Parents):
HPO         Muscle fiber atrophy
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)