Muscle fiber hypertrophy

Symptom Information:

Symptom ID: HPO:0100293
Synonyms:
Muscle fibre hypertrophy [HPO:0100293]
Muscle hypertrophy [Orphanet:44300]
Muscle hypertrophy (MEB) [OMIM:Muscle hypertrophy (MEB)]
Muscle hypertrophy [MedDRA:10028311]
Quality:
Cross references:
HPO:0003712 "Muscle hypertrophy" [Orphanet:44300]
HPO:0003720 "Generalized muscle hypertrophy" [Orphanet:44300]
Orphanet:44300 "Muscle hypertrophy" [Orphanet:44300]
OMIM: "Muscle hypertrophy (MEB)" [OMIM:Muscle hypertrophy (MEB)]
Is a (Direct Parents):
Orphanet Muscle anomalies
HPO         Abnormality of muscle fibers
MedDRA Muscle related signs and symptoms NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle morphology(HPO:0011805)
             Abnormality of muscle fibers(HPO:0004303)
                Muscle fiber hypertrophy(HPO:0100293)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Muscle disorders(MedDRA:10028302)
       Muscle related signs and symptoms NEC(MedDRA:10028326)
          Muscle fiber hypertrophy(HPO:0100293)
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive limb-girdle muscular dystrophy type 2M (Orphanet:206554)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
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)