Kallmann syndrome-heart disease syndrome

MONDO:0016515

Kallmann syndrome with cardiopathy is characterized by hypogonadotropic hypogonadism associated with gonadotropin-releasing hormone (GnRH) deficiency, anosmia or hyposmia (with hypoplasia or aplasia of the olfactory bulbs) and complex congenital cardiac malformations (double-outlet right ventricle, dilated cardiomyopathy, right aortic arch). It represents a distinct clinical entity from Kallmann syndrome.

0 clinical trials for this condition and its sub-types, 0 tagged with Kallmann syndrome-heart disease syndrome itself.

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↑ Multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome (91) ↑ Congenital hypogonadotropic hypogonadism (83)

Including sub-types (0) Tagged with Kallmann syndrome-heart disease syndrome (0)

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