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hypertrophic cardiomyopathy 8

MeSH: C563866ORPHA: 155

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Classification & Codes

Overview

hypertrophic cardiomyopathy that has material basis in homozygous or heterozygous mutation in the MYL3 gene

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

MeSH Code

C563866

Orphanet Code

ORPHA:155
hypertrophic cardiomyopathy 8
MeSHC563866
OrphanetORPHA:155
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO