Generalized muscle hypertrophy
Symptom Information:
Symptom ID: | HPO:0003720 | ||||||
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 hypertrophy(HPO:0003712) Generalized muscle hypertrophy(HPO:0003720) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Muscle disorders(MedDRA:10028302) Muscle related signs and symptoms NEC(MedDRA:10028326) Generalized muscle hypertrophy(HPO:0003720) |
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Database Frequency: | 8 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Autosomal recessive limb-girdle muscular dystrophy type 2M | (Orphanet:206554) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Congenital muscular dystrophy type 1B | (Orphanet:98893) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2 | (OMIM:613150) |
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency | (Orphanet:254864) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Myhre syndrome | (Orphanet:2588) |