Disease #05713 (MYOCOZ (myopathy, congenital with structured cores and Z-line abnormalitie (MYOCOZ)), OMIM:618654)

Official abbreviation MYOCOZ
Name myopathy, congenital with structured cores and Z-line abnormalitie (MYOCOZ)
OMIM ID 618654
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ACTN2
Associated tissues -
Disease features -
Remarks -
Date created 2020-03-29 14:08:06 +02:00 (CEST)
Date last edited 2020-05-03 14:14:32 +02:00 (CEST)


Individuals

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00300292 - - - F no Italy - - - - - MYOCOZ pectus excavatum, ptosis, fatigue, muscle hypotrophy CACNA1S CACNA1S 1 1 Alessandra Govoni
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