hypogonadotropic hypogonadism 17 with or without anosmia

Term ID

DOID:0090079

Synonyms

Definition

A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the SPRY4 gene on chromosome 5q31, sometimes in association with mutations in other genes. https://www.ncbi.nlm.nih.gov/pubmed/23643382

References

• ICD10CM:E23.0
• OMIM:615266

Ontology

Human Disease   ( DOID:0090079 )