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General Information
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| Term |
hypogonadotropic hypogonadism 23 with or without anosmia |
ID (Ontology) |
DOID:0090091 (Human Disease) |
| Definition |
A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the LHB gene on chromosome 19q13. |
| Also Known As |
"46,XY disorder of sex development due to LHB deficiency" ; "46,XY disorder of sex development due to luteinizing hormone subunit beta deficiency" ; "46,XY DSD due to LHB deficiency" (for all, see Synonyms field below) |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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hypogonadotropic hypogonadism 23 with or without anosmia | 1 | for disease ribbon | hypogonadotropic hypogonadism 23 with or without anosmia | 1 | model of | hypogonadotropic hypogonadism 23 with or without anosmia | 1 |
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Relationships