Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
obsolete congenital syphilitic encephalitis	DOID_10795
chronic maxillary sinusitis	DOID_10792	[A maxillary sinusitis which lasts for 12 weeks or more.]
chronic sphenoidal sinusitis	DOID_10793	[A sphenoid sinusitis which lasts for 12 weeks or more.]
hypogonadotropic hypogonadism 19 with or without anosmia	DOID_0090090	[A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the DUSP6 gene on chromosome 12q22, sometimes in association with mutations in other genes.]
hypogonadotropic hypogonadism 21 with or without anosmia	DOID_0090093	[A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the FLRT3 gene on 20p11, sometimes in association with mutations in other genes.]
hypogonadotropic hypogonadism 1 with or without anosmia	DOID_0090094	[A hypogonadotropic hypogonadism that has_material_basis_in mutation in the KAL1 gene on chromosome Xp22.3, sometimes in association with mutation in another gene.]
hypogonadotropic hypogonadism 23 with or without anosmia	DOID_0090091	[A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the LHB gene on chromosome 19q13.]
hypogonadotropic hypogonadism 3 with or without anosmia	DOID_0090092	[A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the PROKR2 gene on chromosome 20p12, sometimes in association with mutation in another gene.]
hypogonadotropic hypogonadism 20 with or without anosmia	DOID_0090082	[A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the FGF17 gene on chromosome 8p21, sometimes in association with mutations in other genes.]
hypogonadotropic hypogonadism 2 with or without anosmia	DOID_0090083	[A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the FGFR1 gene on chromosome 8p11, sometimes in association with mutation in other genes.]
hypogonadotropic hypogonadism 16 with or without anosmia	DOID_0090080	[A hypogonadotropic hypogonadism that has_material_basis_in mutation in the SEMA3A gene on chromosome 7, sometimes in association with mutations in other genes.]
hypogonadotropic hypogonadism 22 with or without anosmia	DOID_0090081	[A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the FEZF1 gene on chromosome 7q31.]
hypogonadotropic hypogonadism 6 with or without anosmia	DOID_0090086	[A hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the FGF8 gene on chromosome 10q24, sometimes in association with mutation in another gene.]
hypogonadotropic hypogonadism 14 with or without anosmia	DOID_0090087	[A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the WDR11 gene on chromosome 10q26.]
hypogonadotropic hypogonadism 5 with or without anosmia	DOID_0090084	[A hypogonadotropic hypogonadism that is characterised by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the CHD7 gene on chromosome 8q12.]
hypogonadotropic hypogonadism 9 with or without anosmia	DOID_0090085	[A hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the NELF gene on chromosome 9q34, sometimes in association with mutation in another gene.]
hypogonadotropic hypogonadism 24 without anosmia	DOID_0090088	[A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the FSHB gene on chromosome 11p14.]
hypogonadotropic hypogonadism 10 with or without anosmia	DOID_0090089	[A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the TAC3 gene on chromosome 12q13.]
hypogonadotropic hypogonadism 11 with or without anosmia	DOID_0090071	[A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the TACR3 gene on chromosome 4q24.]
hypogonadotropic hypogonadism 12 with or without anosmia	DOID_0090072	[A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the GNRH1 gene on chromosome 8p21.]