Phenotypes for disease #01958 (CNM2 (myopathy, centronuclear, type 2 (CNM-2)), OMIM:255200)

8 entries on 1 page. Showing entries 1 - 8.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000117227 reduced fetal movements, oligohydramnios, intra-uterine growth retardation; muscle weakness proximal, slowly progressive, ptosis, contractures at birth, normal intelligence myopathy, centronuclear - Familial, autosomal recessive - - 1d - - Johan den Dunnen 00144462
0000117228 reduced fetal movements, oligohydramnios, intra-uterine growth retardation; muscle weakness proximal, contractures at birth; hypodevelopment frontal lobes; died from viral myocarditis myopathy, centronuclear - Familial, autosomal recessive - - 1d - - Johan den Dunnen 00144463
0000117229 - myopathy, centronuclear - Familial, autosomal recessive - - 00y00m01d - - Johan den Dunnen 00144464
0000117230 normal pregnancy; muscle weakness proximal myopathy, centronuclear - Familial, autosomal recessive - - 8y - - Johan den Dunnen 00144465
0000117231 normal pregnancy; muscle weakness proximal, slowly progressive, facial weakness, ptosis, ophtalmoparesis myopathy, centronuclear - Familial, autosomal recessive - - 1d - - Johan den Dunnen 00144466
0000117232 - myopathy, centronuclear - Familial, autosomal recessive - - - - - Johan den Dunnen 00144495
0000117233 wheelchair-bound 13y myopathy, centronuclear - Unknown - - - - - Johan den Dunnen 00144496
0000117235 centronuclear myopathy; 12y-disease stable myopathy, centronuclear, autosomal recessive - Familial, autosomal recessive 12y - - 5y6m - Johan den Dunnen 00144498
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