All terms in DOID

Label Id Description
mild pre-eclampsia DOID_10590 [A pre-eclampsia characterized by the presence of hypertension without evidence of end-organ damage, in a woman who was normotensive before 20 weeks' gestation.]
pre-eclampsia DOID_10591 [A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy.]
Nannizzia NCBITaxon_1915381
obsolete gonococcal meningitis DOID_10597
obsolete idiopathic neuropathy DOID_10594
neuromuscular disease DOID_440 [A neuropathy that affect the nerves that control the voluntary muscles.]
GM1 gangliosidosis type 3 DOID_0080489 [A GM1 gangliosidosis that is characterized by neurodegeneration and mild skeletal changes and with age at onset ranges from 3 to 30 years.]
Palmoplantar hyperkeratosis HP_0000972
Plantar hyperkeratosis HP_0007556
Palmar hyperkeratosis HP_0010765
Hyperextensible skin HP_0000974
peroxisome biogenesis disorder 11A DOID_0080485 [A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX13 gene on chromosome 2p15.]
Zellweger syndrome DOID_905 [A peroxisomal biogenesis disorder that is characterized by severe neurologic dysfunction, craniofacial abnormalities, and liver dysfunction, and biochemically by the absence of peroxisome and that has_material_basis_in autosomal recessive inheritance of a mutation in the peroxisome biogenesis factor (PEX) genes.]
peroxisome biogenesis disorder 12A DOID_0080486 [A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX19 gene on chromosome 1q23.]
peroxisome biogenesis disorder 13A DOID_0080487 [A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX14 gene on chromosome 1p36.]
trimellitic anhydride CHEBI_53050
cyclic dicarboxylic anhydride CHEBI_36609
2-benzofurans CHEBI_38831
dioxo monocarboxylic acid CHEBI_35951
obsolete localized unresectable neuroblastoma DOID_4172