All terms in DOID

Label Id Description
muscle structure UBERON_0005090
immature cataract DOID_10997 [A senile cataract that is characterized by variable opacification of the lens of the eye with some clear lens fibers remaining.]
senile cataract DOID_9669 [A cataract that is characterized by thickening and loss of transparency of the lens with age progression, caused by a multifactorial etiology related to aging.]
basilar artery UBERON_0001633
branch of vertebral artery UBERON_0035307
head blood vessel UBERON_0003496
acute hemorrhagic leukoencephalitis DOID_10992 [A very rare form of acute disseminated encephalomyelitis, characterized by a brief but intense attack of inflammation and necrotizing vasculitis of venules and hemorrhage, and edema.]
acute disseminated encephalomyelitis DOID_639 [An encephalomyelitis characterized by inflammation located in brain and located in spinal cord that damages myelin. It usually occurs after viral infection, but also following vaccination, bacterial or parasitic infection.]
postinfectious encephalitis DOID_10993 [An encephalitis that is characterized by the immune system mistakenly attacking healthy cells in the brain instead of attacking only the cells causing the infection, often occurring two to three weeks after the initial infection.]
encephalitis DOID_9588 [A brain disease that is characterized as an acute inflammation of the brain with flu-like symptoms.]
autoimmune disease of central nervous system DOID_0060004 [An autoimmune hypersensitivity disease located_in the central nervous system.]
basal ganglia cerebrovascular disease DOID_10991
carotid body UBERON_0001629
nonchromaffin paraganglion UBERON_0034979
obsolete chronic glomerulonephritis with lesion of membranoproliferative glomerulonephritis DOID_10998
Cricetidae NCBITaxon_337677
perivascular space UBERON_0014930
Perlman syndrome DOID_0060476 [A syndrome characterized by polyhydramnios with neonatal macrosomia, nephromegaly, distinctive facial appearance, renal dysplasia, nephroblastomatosis, and predisposition to Wilms tumor. It shows similarities to Beckwith-Wiedemann syndrome.]
Sigmodon alstoni NCBITaxon_134742
Sigmodon NCBITaxon_42414