Disease #01692 (cardiomyopathy, diltaed, with hypergonadotropic hypogonadism (Malouf syndrome), OMIM:212112)

Official abbreviation -
Name cardiomyopathy, diltaed, with hypergonadotropic hypogonadism (Malouf syndrome)
OMIM ID 212112
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene LMNA
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Individuals

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00305350 138383 - - M ? ? (unknown) - - 0 - - cardiomyopathy, diltaed, with hypergonadotropic hypogonadism (Malouf syndrome) Rhabdomyolysis after fitness training, CK > 120000 U/l, declining, no muscle atrophies, no muscle pain; HPO´s: Exercise-induced rhabdomyolysis; Extremely elevated creatine kinase DSP DSP 1 1 Andreas Laner
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