Calf muscle hypertrophy
Symptom Information:
Symptom ID: | HPO:0008981 | |||||||||
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 skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Abnormality of the musculature of the limbs(HPO:0009127) Abnormality of the musculature of the lower limbs(HPO:0001437) Abnormality of the calf musculature(HPO:0001430) Calf muscle hypertrophy(HPO:0008981) Abnormality of the musculature(HPO:0003011) Abnormality of muscle morphology(HPO:0011805) Skeletal muscle hypertrophy(HPO:0003712) Muscle hypertrophy of the lower extremities(HPO:0008968) Calf muscle hypertrophy(HPO:0008981) Abnormality of the musculature of the limbs(HPO:0009127) Abnormality of the musculature of the lower limbs(HPO:0001437) Abnormality of the calf musculature(HPO:0001430) Calf muscle hypertrophy(HPO:0008981) MedDRA: |
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Database Frequency: | 28 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant limb-girdle muscular dystrophy type 1B | (Orphanet:264) |
Autosomal dominant limb-girdle muscular dystrophy type 1C | (Orphanet:265) |
Autosomal dominant limb-girdle muscular dystrophy type 1H | (Orphanet:238755) |
Autosomal recessive limb girdle muscular dystrophy type 2A | (Orphanet:267) |
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
Autosomal recessive limb-girdle muscular dystrophy type 2D | (Orphanet:62) |
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 2I | (Orphanet:34515) |
Autosomal recessive limb-girdle muscular dystrophy type 2L | (Orphanet:206549) |
Autosomal recessive limb-girdle muscular dystrophy type 2M | (Orphanet:206554) |
Becker muscular dystrophy | (Orphanet:98895) |
Cardiomyopathy, dilated, 1X | (OMIM:611615) |
Congenital muscular dystrophy with cerebellar involvement | (Orphanet:370959) |
Duchenne muscular dystrophy | (Orphanet:98896) |
Early-onset myopathy with fatal cardiomyopathy | (Orphanet:289377) |
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1 | (OMIM:158900) |
Facioscapulohumeral dystrophy | (Orphanet:269) |
HYPERTROPHIA MUSCULORUM VERA | (OMIM:145800) |
Hereditary myopathy with lactic acidosis due to ISCU deficiency | (Orphanet:43115) |
Kennedy disease | (Orphanet:481) |
Lower motor neuron syndrome with late-adult onset | (Orphanet:276435) |
MIYOSHI MUSCULAR DYSTROPHY 3 | (OMIM:613319) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 | (OMIM:253800) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 | (OMIM:616052) |
MYOPATHY, DISTAL, INFANTILE-ONSET | (OMIM:160300) |
MYOPATHY, DISTAL, TATEYAMA TYPE | (OMIM:614321) |
Proximal myotonic myopathy | (Orphanet:606) |