Muscle fiber atrophy

Symptom Information:

Symptom ID: HPO:0100295
Synonyms:
Muscle fiber hypotrophy [HPO:0100295]
Muscle atrophy [Orphanet:44250]
Muscle atrophy (disorder) [Orphanet:44250]
Disuse muscle atrophy (disorder) [Orphanet:44250]
Atrophy, Disuse [Orphanet:44250]
Muscular Atrophy [Orphanet:44250]
Muscle hypotrophy/atrophy/dystrophy/agenesis/amyotrophy [Orphanet:44250]
Disuse muscle atrophy [Orphanet:44250]
Amyotrophy [Orphanet:44250]
Muscle atrophy [MedDRA:10028289]
Atrophy muscle [MedDRA:10028289]
Atrophy skeletal muscle [MedDRA:10028289]
Degeneration muscle [MedDRA:10028289]
Disuse muscle atrophy [MedDRA:10028289]
Muscle degeneration [MedDRA:10028289]
Muscle fibrosis atrophy [MedDRA:10028289]
Muscle fibrous atrophy [MedDRA:10028289]
Muscle wasting [MedDRA:10028289]
Muscle wasting (disuse) [MedDRA:10028289]
Muscular wasting and disuse atrophy, not elsewhere classified [MedDRA:10028289]
Amyotrophy [MedDRA:10002027]
Amyotrophy NOS [MedDRA:10002027]
Muscle atrophy (1 patient) [OMIM:Muscle atrophy (1 patient)]
Muscle atrophy (type I) [OMIM:Muscle atrophy (type I)]
Muscle atrophy (variable) [OMIM:Muscle atrophy (variable)]
Muscle wasting (especially legs and arms) [OMIM:Muscle wasting (especially legs and arms)]
Quality:
Cross references:
HPO:0003202 "Amyotrophy" [Orphanet:44250]
HPO:0003700 "Generalized amyotrophy" [Orphanet:44250]
Orphanet:44250 "Muscle hypotrophy/atrophy/dystrophy/agenesis/amyotrophy" [Orphanet:44250]
OMIM: "Muscle atrophy (1 patient)" [OMIM:Muscle atrophy (1 patient)]
OMIM: "Muscle atrophy (type I)" [OMIM:Muscle atrophy (type I)]
OMIM: "Muscle atrophy (variable)" [OMIM:Muscle atrophy (variable)]
OMIM: "Muscle wasting (especially legs and arms)" [OMIM:Muscle wasting (especially legs and arms)]
UMLS:C0264122 "Atrophy, Disuse" [Orphanet:44250]
UMLS:C0026846 "Muscular Atrophy" [Orphanet:44250]
Is a (Direct Parents):
Orphanet Skeletal muscle atrophy
Orphanet Muscle anomalies
HPO         Abnormality of muscle fibers
MedDRA Neuromuscular disorders NEC
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)
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)