Limb-girdle muscular dystrophy
Symptom Information:
Symptom ID: | HPO:0006785 | ||
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) Limb-girdle muscle atrophy(HPO:0003797) Limb-girdle muscular dystrophy(HPO:0006785) MedDRA: |
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Database Frequency: | 14 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant limb-girdle muscular dystrophy type 1G | (Orphanet:55596) |
Autosomal recessive limb-girdle muscular dystrophy type 2C | (Orphanet:353) |
Autosomal recessive limb-girdle muscular dystrophy type 2D | (Orphanet:62) |
Autosomal recessive limb-girdle muscular dystrophy type 2E | (Orphanet:119) |
Autosomal recessive limb-girdle muscular dystrophy type 2F | (Orphanet:219) |
Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
Autosomal recessive limb-girdle muscular dystrophy type 2M | (Orphanet:206554) |
Autosomal recessive limb-girdle muscular dystrophy type 2Q | (Orphanet:254361) |
Autosomal recessive limb-girdle muscular dystrophy type 2S | (Orphanet:369840) |
Emery-Dreifuss muscular dystrophy | (Orphanet:261) |
Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 3 | (OMIM:615424) |
MUSCULAR DYSTROPHY, HEMIZYGOUS LETHAL TYPE | (OMIM:309950) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 | (OMIM:616052) |