hypertrophic cardiomyopathy 3

MeSH: C566170ORPHA: 155

Overview

hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22

Available Treatments (0)

No treatments linked yet

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

Classification & Codes

MeSH Code

C566170

Orphanet Code

ORPHA:155
hypertrophic cardiomyopathy 3
MeSHC566170
OrphanetORPHA:155
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
hypertrophic cardiomyopathy 3 | OrphanDrug