Generalized amyotrophy

Symptom Information:

Symptom ID: HPO:0003700
Synonyms:
Diffuse amyotrophy [HPO:0003700]
Diffuse muscle atrophy [HPO:0003700]
Diffuse muscle wasting [HPO:0003700]
Diffuse skeletal muscle wasting [HPO:0003700]
Generalized muscle atrophy [HPO:0003700]
Muscle atrophy, diffuse [HPO:0003700]
Muscle atrophy, generalized [HPO:0003700]
Muscular atrophy, generalized [HPO:0003700]
Amyotrophy [Orphanet:44250]
Muscle atrophy [Orphanet:44250]
Muscle atrophy (disorder) [Orphanet:44250]
Disuse muscle atrophy (disorder) [Orphanet:44250]
Muscular Atrophy [Orphanet:44250]
Atrophy, Disuse [Orphanet:44250]
Diffuse muscle atrophy [OMIM:Diffuse muscle atrophy]
Generalized amyotrophy [OMIM:Generalized amyotrophy]
Generalized muscle atrophy [OMIM:Generalized muscle atrophy]
Muscle atrophy, diffuse [OMIM:Muscle atrophy, diffuse]
Muscle atrophy, generalized [OMIM:Muscle atrophy, generalized]
Muscular atrophy, generalized [OMIM:Muscular atrophy, generalized]
Muscle hypotrophy/atrophy/dystrophy/agenesis/amyotrophy [Orphanet:44250]
Disuse muscle atrophy [Orphanet:44250]
Amyotrophy [MedDRA:10002027]
Amyotrophy NOS [MedDRA:10002027]
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]
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:0100295 "Muscle fiber atrophy" [Orphanet:44250]
Orphanet:44250 "Muscle hypotrophy/atrophy/dystrophy/agenesis/amyotrophy" [Orphanet:44250]
OMIM: "Diffuse muscle atrophy" [OMIM:Diffuse muscle atrophy]
OMIM: "Generalized amyotrophy" [OMIM:Generalized amyotrophy]
OMIM: "Generalized muscle atrophy" [OMIM:Generalized muscle atrophy]
OMIM: "Muscle atrophy, diffuse" [OMIM:Muscle atrophy, diffuse]
OMIM: "Muscle atrophy, generalized" [OMIM:Muscle atrophy, generalized]
OMIM: "Muscular atrophy, generalized" [OMIM:Muscular atrophy, generalized]
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:C0026846 "Muscular Atrophy" [Orphanet:44250]
UMLS:C0264122 "Atrophy, Disuse" [Orphanet:44250]
Is a (Direct Parents):
MedDRA Neuromuscular disorders NEC
HPO         Skeletal muscle atrophy
Orphanet Skeletal muscle atrophy
Orphanet Muscle anomalies
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)
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)