Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
cardia cancer	DOID_10548
cardia of stomach	UBERON_0001162
gastric cardia adenocarcinoma	DOID_6271
obsolete wrist or carpus enthesopathy	DOID_10473
inflammatory breast carcinoma	DOID_6263	[A breast adenocarcinoma that is characterized by the clinical appearance of inflammation, with edema and redness of the breast due to pathologic plugging of the dermal lymphatics of the breast with tumor emboli.]
Pneumocystidomycetes	NCBITaxon_147553
obsolete recurrent pediatric medulloblastoma	DOID_7593
follicular dendritic cell sarcoma	DOID_6262	[A dendritic cell sarcoma cancer that effects the follicular dendritic cells.]
dendritic cell sarcoma	DOID_7849	[A histiocytic and dendritic cell cancer that is mainly located_in lymph nodes.]
follicular dendritic cell	CL_0000442
cervical lymphoepithelioma-like carcinoma	DOID_7598	[A cervical squamous cell carcinoma that is characterized by poorly defined islands of undifferentiated squamous cells in a background intensely infi ltrated by lymphocytes. The tumour cells have uniform, vesicular nuclei with prominent nucleoli and moderate amounts of slightly eosinophilic cytoplasm. The cell borders are indistinct.]
lymphoepithelioma-like thymic carcinoma	DOID_7599
obsolete recurrent extraskeletal chondrosarcoma	DOID_6268
asbestos-related lung carcinoma	DOID_7596
allodynia	SYMP_0000840	[Allodynia is a pain where there is a painful sensation with a normal, non painful stimulation.]
nephrotic syndrome type 18	DOID_0080393	[A familial nephrotic syndrome that has_material_basis_in by homozygous or compound heterozygous mutation in the NUP133 gene on chromosome 1q42.]
reactive hyperemia	SYMP_0000841	[Reactive hyperemia is a hyperemia occuring due to the dilation of arteriolar smooth muscle to increase blood flow in response to a profound increase in blood flow to an organ after being occluded. There will be a shortage of oxygen and a build-up of metabolic waste.]
nephrotic syndrome type 19	DOID_0080394	[A familial nephrotic syndrome that has_material_basis_in compound heterozygous mutation in the NUP160 gene on chromosome 11p11.]
orofacial cleft 1	DOID_0080395	[An orofacial cleft characterized by autosomal dominant inheritance that has_material_basis_in variation in chromosome region 6p24.3.]
orofacial cleft 2	DOID_0080396	[An orofacial cleft that has_material_basis_in variation in the chromosome region 2p13.]