All terms in DOID

Label Id Description
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.]
rigidity hypokinesia SYMP_0000859 [Rigidity hypokinesia a type of hypokinesia described as the increase in muscle tension when moved by an outside force.]
hypokinesia SYMP_0000858 [Hypokinesia is a musculoskeletal system symptom characterized by the slow or diminished movement of body musculature. It may be associated with basal ganglia diseases; mental disorders; prolonged inactivity due to illness; experimental protocols used to evaluate the physiologic effects of immobility; and other conditions.]
sex cord-stromal benign neoplasm DOID_0080368 [A reproductive organ benign neoplasm that arises in the ovary or testis and that is composed of granulosa cells, Leydig cells, Sertoli cells, and/or fibroblasts.]
obsolete hypertonic, incoordinate, or prolonged uterine contractions DOID_10483
ovarian sex-cord stromal tumor DOID_0080369 [A sex cord-gonadal stromal tumor that arises from the ovary and is composed of granulosa cells, Sertoli cells, Leydig cells, theca cells, and fibroblasts.]
diaphragmatic eventration DOID_10480
objective vertigo SYMP_0000857 [A vertigo that is characterized by a sensation that the external world is revolving.]