All terms in DOID

Label Id Description
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.]
Pneumocystomycetes NCBITaxon_147553
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.]
obsolete recurrent pediatric medulloblastoma DOID_7593
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 [A pain that is characterized by 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 occurring 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.]
nephrotic syndrome type 1 DOID_0080390 [A familial nephrotic syndrome characterized by prenatal onset of massive proteinuria followed by steroid resistant renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the NPHS1 gene on chromosome 19q13.]
nephrotic syndrome type 9 DOID_0080391 [A familial nephrotic syndrome characterized by steroid-resistant proteinuria, hypoalbuminemia and edema with onset in the first or second decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the COQ8B gene on chromosome 19q13.]
nephrotic syndrome type 17 DOID_0080392 [A familial nephrotic syndrome that has_material_basis_in by homozygous or compound heterozygous mutation in the NUP85 gene on chromosome 17q25.]