FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hypogonadotropic hypogonadism 21 with or without anosmia ID (Ontology) DOID:0090093 (Human Disease)
Definition A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the FLRT3 gene on 20p11, sometimes in association with mutations in other genes.
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 hypogonadotropic hypogonadism 21 with or without anosmia       1
 for disease ribbon | hypogonadotropic hypogonadism 21 with or without anosmia       1
 model of | hypogonadotropic hypogonadism 21 with or without anosmia       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease_____
hypogonadism                       |
 |__hypogonadotropic hypogonadism__|
                                   hypogonadotropic hypogonadism 21 with or without anosmia  1 rec.
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Is a autosomal dominant disease
hypogonadotropic hypogonadism
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ICD10CM:E23.0
MIM:615271