Pelvic girdle muscle atrophy
Symptom Information:
Symptom ID: | HPO:0008988 | ||||
Synonyms: |
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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 the musculature of the pelvis(HPO:0001469) Aplasia/Hypoplasia of the musculature of the pelvis(HPO:0001471) Pelvic girdle muscle atrophy(HPO:0008988) Abnormality of the hip-girdle musculature(HPO:0001445) Pelvic girdle muscle atrophy(HPO:0008988) MedDRA: |
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Database Frequency: | 5 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal recessive Emery-Dreifuss muscular dystrophy | (Orphanet:98855) |
Autosomal recessive limb-girdle muscular dystrophy type 2E | (Orphanet:119) |
Autosomal recessive limb-girdle muscular dystrophy type 2H | (Orphanet:1878) |
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia | (Orphanet:52430) |
X-linked Emery-Dreifuss muscular dystrophy | (Orphanet:98863) |