Phenotypes for disease #01692 (cardiomyopathy, diltaed, with hypergonadotropic hypogonadism (Malouf syndrome), OMIM:212112)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000231200 Rhabdomyolysis after fitness training, CK > 120000 U/l, declining, no muscle atrophies, no muscle pain; HPO´s: Exercise-induced rhabdomyolysis; Extremely elevated creatine kinase - - Unknown 31y - - - - Andreas Laner 00305350
0000301666 best corrected visual acuity: 1.5; electroretinogram , rod: mildly reduced, cone: mildly reduced - dystrophy, corneoretinal, crystalline, Bietti (BCD) Familial, autosomal recessive 55y - - - - LOVD 00409549
0000311636 dilated cardiomyopathy - - Familial, autosomal dominant - - - - - Yi-Qing Yang 00420368
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