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Human Disease
hypogonadotropic hypogonadism 4 with or without anosmia
- Term ID
- DOID:0090077
- Synonyms
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- Definition
- A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the prokineticin-2 gene (PROK2) on chromosome 3p13, sometimes in association with mutation in another gene. (2)
- References
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- ICD10CM:E23.0
- MIM:610628
- Ontology
- Human Disease ( DOID:0090077 )
- is a type of
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