Proximal amyotrophy

Symptom Information:

Symptom ID: HPO:0007126
Synonyms:
Muscle atrophy, proximal [HPO:0007126]
Proximal muscle atrophy [HPO:0007126]
Proximal muscle wasting [HPO:0007126]
Symmetric proximal muscular atrophy [HPO:0007126]
Symmetrical, proximal limb muscle atrophy [HPO:0007126]
Muscle atrophy, proximal [OMIM:Muscle atrophy, proximal]
Proximal muscle atrophy [OMIM:Proximal muscle atrophy]
Proximal muscle wasting [OMIM:Proximal muscle wasting]
Symmetric proximal muscular atrophy [OMIM:Symmetric proximal muscular atrophy]
Symmetrical, proximal limb muscle atrophy (pelvic, scapular, trunk muscles) [OMIM:Symmetrical, proximal limb muscle atrophy (pelvic, scapular, trunk muscles)]
Quality:
Cross references:
OMIM: "Muscle atrophy, proximal" [OMIM:Muscle atrophy, proximal]
OMIM: "Proximal muscle atrophy" [OMIM:Proximal muscle atrophy]
OMIM: "Proximal muscle wasting" [OMIM:Proximal muscle wasting]
OMIM: "Symmetric proximal muscular atrophy" [OMIM:Symmetric proximal muscular atrophy]
OMIM: "Symmetrical, proximal limb muscle atrophy (pelvic, scapular, trunk muscles)" [OMIM:Symmetrical, proximal limb muscle atrophy (pelvic, scapular, trunk muscles)]
Is a (Direct Parents):
HPO         Skeletal muscle 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)
             Skeletal muscle atrophy(HPO:0003202)
                Proximal amyotrophy(HPO:0007126)
MedDRA:
Database Frequency: 29 / 7739
Resource:

All diseases associated with this symptom:

AMYOTROPHIC LATERAL SCLEROSIS 6, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA (OMIM:608030)
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency (Orphanet:329314)
Autosomal dominant Emery-Dreifuss muscular dystrophy (Orphanet:98853)
Autosomal recessive limb girdle muscular dystrophy type 2A (Orphanet:267)
Autosomal recessive limb-girdle muscular dystrophy type 2E (Orphanet:119)
Autosomal recessive limb-girdle muscular dystrophy type 2F (Orphanet:219)
Congenital muscular dystrophy with cerebellar involvement (Orphanet:370959)
Congenital myasthenic syndromes with glycosylation defect (Orphanet:353327)
EMERY-DREIFUSS MUSCULAR DYSTROPHY 4, AUTOSOMAL DOMINANT (OMIM:612998)
EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT (OMIM:612999)
EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT (OMIM:614302)
Ehlers-Danlos syndrome due to tenascin-X deficiency (Orphanet:230839)
Hereditary motor and sensory neuropathy, Okinawa type (Orphanet:90117)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 (OMIM:606612)
MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE (OMIM:159400)
MYASTHENIC SYNDROME, CONGENITAL, 10 (OMIM:254300)
MYASTHENIC SYNDROME, CONGENITAL, 12 (OMIM:610542)
Myasthenia gravis (Orphanet:589)
Myopathy and diabetes mellitus (Orphanet:2596)
NEMALINE MYOPATHY 5 (OMIM:605355)
PLEOCONIAL MYOPATHY WITH SALT CRAVING (OMIM:262900)
Postsynaptic congenital myasthenic syndromes (Orphanet:98913)
Progressive external ophthalmoplegia - myopathy - emaciation (Orphanet:352447)
Proximal spinal muscular atrophy (Orphanet:70)
Proximal spinal muscular atrophy type 4 (Orphanet:83420)
SPINAL MUSCULAR ATROPHY, RYUKYUAN TYPE (OMIM:271200)
Spheroid body myopathy (Orphanet:268129)
Tubular aggregate myopathy (Orphanet:2593)
X-linked Emery-Dreifuss muscular dystrophy (Orphanet:98863)