Skeletal muscle hypertrophy

Symptom Information:

Symptom ID: HPO:0003712
Synonyms:
Hypertrophic muscles [HPO:0003712]
Muscular hypertrophy [HPO:0003712]
Hypertrophic muscles [OMIM:Hypertrophic muscles]
Muscle hypertrophy [OMIM:Muscle hypertrophy]
Muscular hypertrophy [OMIM:Muscular hypertrophy]
Muscle hypertrophy [Orphanet:44300]
Muscle hypertrophy (MEB) [OMIM:Muscle hypertrophy (MEB)]
Muscle hypertrophy [MedDRA:10028311]
Quality:
Cross references:
HPO:0003720 "Generalized muscle hypertrophy" [Orphanet:44300]
HPO:0100293 "Muscle fiber hypertrophy" [Orphanet:44300]
Orphanet:44300 "Muscle hypertrophy" [Orphanet:44300]
OMIM: "Hypertrophic muscles" [OMIM:Hypertrophic muscles]
OMIM: "Muscle hypertrophy" [OMIM:Muscle hypertrophy]
OMIM: "Muscular hypertrophy" [OMIM:Muscular hypertrophy]
OMIM: "Muscle hypertrophy (MEB)" [OMIM:Muscle hypertrophy (MEB)]
Is a (Direct Parents):
HPO         Facial muscle hypertrophy
MedDRA Muscle related signs and symptoms NEC
HPO         Paraspinal muscle hypertrophy
Orphanet Muscle anomalies
HPO         Neck muscle hypertrophy
HPO         Abnormality of muscle morphology
HPO         Scapular muscle hypertrophy
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)
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)