Proximal amyotrophy
Symptom Information:
Symptom ID: | HPO:0007126 | ||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |