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Metadata
ID	DOID:0090088
Name	hypogonadotropic hypogonadism 24 without anosmia
Definition	A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the FSHB gene on chromosome 11p14. https://www.ncbi.nlm.nih.gov/pubmed/8220432, https://www.ncbi.nlm.nih.gov/pubmed/9271483
Xrefs	ICD10CM:E23.6 OMIM:229070 ORDO:52901
Subsets	DO_rare_slim
Synonyms	isolated follicle-stimulating hormone deficiency [EXACT]
Parent Relationships	is_a hypogonadotropic hypogonadism is_a autosomal recessive disease