Search Ontology:
Human Disease
hypogonadotropic hypogonadism 22 with or without anosmia
- Term ID
- DOID:0090081
- Synonyms
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- Definition
- A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the FEZF1 gene on chromosome 7q31. https://www.ncbi.nlm.nih.gov/pubmed/25192046
- References
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- ICD10CM:E23.0
- MIM:616030
- Ontology
- Human Disease ( DOID:0090081 )
- is a type of
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Zebrafish Models