All terms in DOID

Label Id Description
spermatogenic failure 28 DOID_0111916 [A spermatogenic failure characterized by nonobstructive azoospermia and a Sertoli cell-only phenotype in testes that has_material_basis_in homozygous or compound heterozygous mutation in the FANCM gene on chromosome 14q21.2.]
obsolete metastasis to the retina DOID_772
spermatogenic failure 43 DOID_0111917 [A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in absence of forward motility in spermatozoa and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the SPEF2 gene on chromosome 5p13.2.]
retinal cell cancer DOID_771 [A malignant neoplasm that derives_from the retina.]
spermatogenic failure 35 DOID_0111914 [A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in severely impaired sperm motility and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the QRICH2 gene on chromosome 17q25.1.]
Strongyloides stercoralis NCBITaxon_6248
Strongyloides NCBITaxon_6247
spermatogenic failure 33 DOID_0111915 [A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella resulting in immotile spermatozoa and infertility that has_material_basis_in homozygous or compound heterozygous mutation in the WDR66 gene on chromosome 12q24.31.]
Strongyloididae NCBITaxon_6246
spermatogenic failure 41 DOID_0111912 [A spermatogenic failure characterized by oligozoospermia and multiple morphologic abnormalities of the flagella that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP70 gene on chromosome 10q22.2.]
spermatogenic failure 30 DOID_0111913 [A spermatogenic failure characterized by nonobstructive azoospermia or cryptozoospermia that has_material_basis_in homozygous or compound heterozygous mutation in the TDRD9 gene on chromosome 14q32.33.]
intraocular lymphoma DOID_775
bisphenol A CHEBI_33216 [A bisphenol that is 4,4'-methanediyldiphenol in which the methylene hydrogens are replaced by two methyl groups.]
autosomal dominant thrombophilia due to protein S deficiency DOID_0111900 [A protein S deficiency characterized by reduced serum protein S levels and recurrent venous thrombosis that has_material_basis_in heterozygous mutation in the PROS1 gene on chromosome 3q11.1.]
thrombophilia due to thrombin defect DOID_0111907 [A thrombophilia characterized by recurrent thrombophilia that has_material_basis_in heterozygous mutation in F2 on chromosome 11p11.2.]
obsolete meningococcal carditis DOID_763
suprofen CHEBI_9362
thrombophilia due to thrombomodulin defect DOID_0111908 [A thrombophilia characterized by increased risk of developing arterial but not venous thrombosis that has_material_basis_in mutation in the THBD gene on chromosome 20p11.21.]
obsolete bacterial endocarditis DOID_762
autosomal recessive thrombophilia due to protein S deficiency DOID_0111905 [A protein S deficiency characterized by thrombosis and secondary hemorrhage usually beginning in early infancy that has_material_basis_in homozygous or compound heterozygous mutation in the PROS1 gene on chromosome 3q11.1.]