- OMIM ID
-
212112
- OMIM term:
- CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTROPIC HYPOGONADISM
- Alternative terms:
-
MALOUF SYNDROME
CARDIOMYOPATHY, CONGESTIVE, WITH HYPERGONADOTROPIC HYPOGONADISM
CARDIOMYOPATHY, DILATED, WITH PREMATURE OVARIAN FAILURE
CARDIOMYOPATHY WITH PRIMARY TESTICULAR FAILURE
NAJJAR SYNDROME
GENITAL ANOMALY WITH CARDIOMYOPATHY
CARDIOGENITAL SYNDROME
- (∗) Location:
- 1q22
- (†) Associated OMIM genes:
- LMNA
- (‡) Associated MGI genes:
Loading mouse genes ...