Dilate kardiyomiyopati-hipergonadotropik hipogonadizm sendromu
ORPHA:2229· ICD-10 I42.0· Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
- Yaygınlık
- <1 / 1 000 000
- Kalıtım
- Autosomal recessive
- Başlangıç yaşı
- Infancy, Neonatal
ORPHA:2229· ICD-10 I42.0· Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome