All terms in DOID

Label Id Description
synovial joint of pelvic girdle UBERON_0011107
joint of girdle UBERON_0008114
synovial joint UBERON_0002217
great vessel of heart UBERON_0013768
blood vessel UBERON_0001981
horned turban snail allergy DOID_0060531 [A snail allergy triggered by the horned turban snail.]
snail allergy DOID_0060530 [A mollusc allergy triggered by snails.]
latex allergy DOID_0060532 [An allergic disease that is triggered by latex.]
nerve of head region UBERON_0011779
nerve UBERON_0001021
cranial neuron projection bundle UBERON_0034713
hepatoid adenocarcinoma DOID_0060534 [An adenocarcinoma with morphologic characteristics similar to hepatocellular carcinoma, arising from an anatomic site other than the liver.]
adenocarcinoma DOID_299 [A carcinoma that has_material_basis_in abnormally proliferating cells, derives_from epithelial cells, which originate in glandular tissue.]
Warsaw breakage syndrome DOID_0060535 [A syndrome mainly characterized by severe congenital microcephaly, growth restriction, and sensorineural hearing loss due to cochlear hypoplasia and that has_material_basis_in homozygous or compound heterozygous mutation in the DDX11 gene on chromosome 12p11.]
mitochondrial complex I deficiency DOID_0060536 [A mitochondrial metabolism disease characterized by a wide range of manifestations including marked and often fatal lactic acidosis, cardiomyopathy, leukoencephalopathy, pure myopathy and hepatopathy with tubulopathy. Among the numerous clinical phenotypes observed are Leigh syndrome, Leber hereditary optic neuropathy and MELAS syndrome. It can have material basis in mutations in multiple different genes, both nuclear-encoded and mitochondrial-encoded.]
mitochondrial metabolism disease DOID_700 [An inherited metabolic disorder that involves mitochondrial metabolism dysfunction.]
mitochondrial complex II deficiency DOID_0060537 [A mitochondrial metabolism disease characterized by a highly variable phenotype. Some patients have multisystem involvement of the brain, heart, muscle, liver, and kidneys resulting in death in infancy, whereas others have only isolated cardiac or muscle involvement with onset in adulthood and normal cognition. It has_material_basis_in homozygous or compound heterozygous mutation in the nuclear-encoded SDHA gene on chromosome 5p, the nuclear-encoded SDHAF1 gene on chromosome 19q, or the nuclear-encoded SDHD gene on chromosome 11q23.]
purpura fulminans DOID_0060538 [A purpura characterized by blood spots, bruising and discoloration of the skin resulting from coagulation in small blood vessels within the skin and rapidly leading to skin necrosis and disseminated intravascular coagulation. It is often fatal.]
purpura DOID_3326
transient arthritis DOID_2092