Disease #01226 (CMH4 (cardiomyopathy, hypertrophic, familial, type 4 (CMH-4)), OMIM:115197)

Official abbreviation CMH4
Name cardiomyopathy, hypertrophic, familial, type 4 (CMH-4)
OMIM ID 115197
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MYBPC3
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

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00051500 - - - M no (Italy) white - - - - CMH4 hypetropy of left ventricle MYBPC3 MYBPC3 1 1 Domenico Coviello
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