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Kallmann syndrome

Disease Summary
Associated Targets (34)
Tbio

25

Tchem

7

Tclin

2


Explore Associated Targets
Mondo Description Kallmann syndrome (KS) is a developmental genetic disorder characterized by the association of congenital hypogonadotropic hypogonadism (CHH) due to gonadotropin-releasing hormone (GnRH) deficiency, and anosmia or hyposmia (with hypoplasia or aplasia of the olfactory bulbs).
Disease Ontology Description A hypogonadotropic hypogonadism with a defective sense of smell (anosmia or hyposmia).
Mondo Term and Equivalent IDs
MONDO:0018800:  Kallmann syndrome
GARD:0010771: 
MESH:D017436: 
NCIT:C75479: 
Orphanet:478: 
SCTID:93559003: 
UMLS:C0162809: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Target Novelty (Tin-x)