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| Term | hypogonadotropic hypogonadism 13 with or without anosmia | ID (Ontology) | DOID:0090073 (Human Disease) |
| Definition | A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the KISS1 gene on chromosome 1q32. | ||
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autosomal genetic disease |__autosomal recessive disease____ hypogonadism | |__hypogonadotropic hypogonadism__| hypogonadotropic hypogonadism 13 with or without anosmia |
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autosomal recessive disease hypogonadotropic hypogonadism |
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ICD10CM:E23.0 MIM:614842 |
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