| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_3614) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D017436 |
| Similar Terms | |
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6 genes/proteins associated with the disease Kallmann Syndrome from the curated CTD Gene-Disease Associations dataset.
