Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
Spirochaetales	NCBITaxon_136
Spirochaetia	NCBITaxon_203692
Borreliella burgdorferi	NCBITaxon_139
Borreliella	NCBITaxon_64895
Borrelia	NCBITaxon_138
Borreliaceae	NCBITaxon_1643685
Hermansky-Pudlak syndrome 1	DOID_0060539	[A Hermansky-Pudlak syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the HPS1 gene on chromosome 10q24.]
great vessel of heart	UBERON_0013768
blood vessel	UBERON_0001981
horned turban snail allergy	DOID_0060531
snail allergy	DOID_0060530	[A mollusc allergy triggered by snails.]
Turbo cornutus	NCBITaxon_63673
latex allergy	DOID_0060532	[A hypersensitivity reaction type I disease triggered by latex.]
Hevea brasiliensis	NCBITaxon_3981
nerve of head region	UBERON_0011779
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.]