hypogonadotropic hypogonadism 18 with or without anosmia

Term ID

DOID:0090076

Synonyms

Definition

A hypogonadotropic hypogonadism that has_material_basis_in heterozygous or homozygous mutation in the IL17RD gene on chromosome 3p14, sometimes in association with mutation in other genes. https://www.ncbi.nlm.nih.gov/pubmed/23643382

References

ICD10CM:E23.0
MIM:615267

Ontology

Human Disease ( DOID:0090076 )

Relationships

is a type of: autosomal dominant disease autosomal recessive disease hypogonadotropic hypogonadism

autosomal dominant disease autosomal recessive disease hypogonadotropic hypogonadism Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models