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Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome

Disease Export to PDF
Name:
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
Description:
This syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH).
ORPHAcode:
2229
Synonyms:
Cardiogenital syndrome
Malouf syndrome
Najjar syndrome
XREF(s):
Orphanet
ICD-10
OMIM
Analyte(s):
LMNA
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14