Search Ontology:
Human Disease
hypogonadotropic hypogonadism 1 with or without anosmia
- Term ID
- DOID:0090094
- Synonyms
-
- dysplasia olfactogenitalis of de morsier
- Definition
- A hypogonadotropic hypogonadism that has_material_basis_in mutation in the KAL1 gene on chromosome Xp22.3, sometimes in association with mutation in another gene. (3)
- References
-
- ICD10CM:E23.0
- MIM:308700
- Ontology
- Human Disease ( DOID:0090094 )
- is a type of
Other Pages
Genes Involved
Human Gene | Zebrafish Ortholog | OMIM Term | Disease | OMIM Phenotype ID |
---|---|---|---|---|
ANOS1 | Hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1) | hypogonadotropic hypogonadism 1 with or without anosmia | 308700 |
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