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 Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 3
Associated with 1 gene LMNA
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00305350 138383 - - M ? - - - - - - 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
00409549 K6026 PubMed: Oishi 2018 - F - Japan - - - - - cardiomyopathy, diltaed, with hypergonadotropic hypogonadism (Malouf syndrome) best corrected visual acuity: 1.5; electroretinogram , rod: mildly reduced, cone: mildly reduced CYP4V2 CYP4V2 1 1 LOVD
00417576 - - - - - - - - - - - cardiomyopathy, diltaed, with hypergonadotropic hypogonadism (Malouf syndrome) - ABCC9 ABCC9 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00420368 - - - - no - - - - - - cardiomyopathy, diltaed, with hypergonadotropic hypogonadism (Malouf syndrome) dilated cardiomyopathy - BMP10 1 1 Yi-Qing Yang
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