Skeletal muscle hypertrophy
Symptom Information:
Symptom ID: | HPO:0003712 | ||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): | |||||||||
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) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Muscle disorders(MedDRA:10028302) Muscle related signs and symptoms NEC(MedDRA:10028326) Skeletal muscle hypertrophy(HPO:0003712) |
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Database Frequency: | 42 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Acetazolamide-responsive myotonia | (Orphanet:99736) |
Autosomal dominant centronuclear myopathy | (Orphanet:169189) |
Autosomal dominant cervical dystonia | (Orphanet:93962) |
Autosomal dominant focal dystonia, DYT7 type | (Orphanet:93963) |
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 2M | (Orphanet:206554) |
Autosomal recessive limb-girdle muscular dystrophy type 2N | (Orphanet:206559) |
Autosomal recessive limb-girdle muscular dystrophy type 2O | (Orphanet:206564) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Familial partial lipodystrophy associated with PLIN1 mutations | (Orphanet:280356) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Hemihypertrophy | (Orphanet:2128) |
Hyperkalemic periodic paralysis | (Orphanet:682) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
Léri-Weill dyschondrosteosis | (Orphanet:240) |
MASTICATORY MUSCLES, HYPERTROPHY OF | (OMIM:154850) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2 | (OMIM:613150) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 2 | (OMIM:613156) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 6 | (OMIM:608840) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 | (OMIM:606612) |
MYOTONIA CONGENITA, AUTOSOMAL DOMINANT | (OMIM:160800) |
MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE | (OMIM:255700) |
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency | (Orphanet:254864) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Muscular pseudohypertrophy - hypothyroidism | (Orphanet:2349) |
Myhre syndrome | (Orphanet:2588) |
Myostatin-related muscle hypertrophy | (Orphanet:275534) |
Myotonia fluctuans | (Orphanet:99734) |
Myotonia permanens | (Orphanet:99735) |
Paramyotonia congenita of Von Eulenburg | (Orphanet:684) |
Parkes Weber syndrome | (Orphanet:90307) |
Potassium-aggravated myotonia | (Orphanet:612) |
Primary lipodystrophy | (Orphanet:90970) |
RIPPLING MUSCLE DISEASE | (OMIM:606072) |
RIPPLING MUSCLE DISEASE 1 | (OMIM:600332) |
Richieri Costa-da Silva syndrome | (Orphanet:3101) |
Rippling muscle disease | (Orphanet:97238) |
SATOYOSHI SYNDROME | (OMIM:600705) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Thomsen and Becker disease | (Orphanet:614) |