Calf muscle hypertrophy

Symptom Information:

Symptom ID: HPO:0008981
Synonyms:
Calf hypertrophy [HPO:0008981]
Muscular hypertrophy of the calf muscles [HPO:0008981]
Calf hypertrophy [OMIM:Calf hypertrophy]
Calf muscle hypertrophy [OMIM:Calf muscle hypertrophy]
Calf hypertrophy (early in the disease) [OMIM:Calf hypertrophy (early in the disease)]
Calf hypertrophy (in some patients) [OMIM:Calf hypertrophy (in some patients)]
Calf hypertrophy (less common) [OMIM:Calf hypertrophy (less common)]
Calf hypertrophy (reported in 1 family) [OMIM:Calf hypertrophy (reported in 1 family)]
Calf hypertrophy (uncommon) [OMIM:Calf hypertrophy (uncommon)]
Quality:
Cross references:
OMIM: "Calf hypertrophy" [OMIM:Calf hypertrophy]
OMIM: "Calf muscle hypertrophy" [OMIM:Calf muscle hypertrophy]
OMIM: "Calf hypertrophy (early in the disease)" [OMIM:Calf hypertrophy (early in the disease)]
OMIM: "Calf hypertrophy (in some patients)" [OMIM:Calf hypertrophy (in some patients)]
OMIM: "Calf hypertrophy (less common)" [OMIM:Calf hypertrophy (less common)]
OMIM: "Calf hypertrophy (reported in 1 family)" [OMIM:Calf hypertrophy (reported in 1 family)]
OMIM: "Calf hypertrophy (uncommon)" [OMIM:Calf hypertrophy (uncommon)]
Is a (Direct Parents):
HPO         Abnormality of the calf musculature
HPO         Muscle hypertrophy of the lower extremities
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)
                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)
       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)
MedDRA:
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)