All terms in DOID

Label Id Description
cerebrovascular benign neoplasm DOID_60007 [A cardiovascular organ benign neoplasm that is located_in the cerebrovascular system.]
mydriasis SYMP_0000396
dilated pupil SYMP_0000254
childhood choroid plexus cancer DOID_3545
obsolete inherited blood coagulation disease DOID_2214
breast adenoid cystic carcinoma DOID_4877 [A breast carcinoma that is characterized by the presence of a dual cell population of luminal and basaloid cells arranged in specific growth patterns.]
unreactive mydriasis SYMP_0000397
tracheal cancer DOID_11920 [A respiratory system cancer that is located_in the trachea.]
factor VII deficiency DOID_2215 [A blood coagulation disease that is characterized by easy bleeding, has_symptom epistaxis, bleeding of the gums, menorrhagia, and occasionally hemarthrosis, and has_material_basis_in autosomal recessive inheritance of mutation in the F7 gene, which encodes coagulation factor VII, an important factor in the clotting cascade.]
obsolete somatosensory disorder DOID_3546
muscle twitching SYMP_0000394
Bartholin's gland adenoid cystic carcinoma DOID_4879 [A Bartholin's gland carcinoma that is characterized by a distinctive pattern in which abnormal nests and columns of cells of bland appearance are arranged concentrically around glandlike spaces filled with eosinophilic periodic acid-Schiff-positive diastase-resistant material.]
factor V deficiency DOID_2216
facial muscle twitching SYMP_0000395
Bernard-Soulier syndrome DOID_2217 [A blood coagulation disease characterized by autosomal recessive inheritance of mucosal bleeding, purpuric skin bleeding, epistaxis, and menorrhagia with prolonged bleeding times, enlarged platelets and absence of platelet aggregation in response to von Willebrand factor that has_material_basis_in mutation in the GP1BA gene, the GP1BB gene, or the GP9 gene which are subunits of the platelet membrane von Willebrand factor receptor complex, glycoprotein Ib.]
esophageal adenoid cystic carcinoma DOID_4878 [An esophageal carcinoma that derives_from epithelial cells of the salivary gland.]
factor XI deficiency DOID_2229 [A hemophilia that is characterized by deficiency of factor XI clotting factor and mild prolonged bleeding, especially of mucosal sites following trauma, and has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation of the coagulation factor XI gene of chromosome 4q35.2.]
hemophilia DOID_0061030 [A blood coagulation disease characterized by spontaneous hemorrhage or prolonged bleeding.]
kidney clear cell sarcoma DOID_4880 [A kidney sarcoma that has_material_basis_in clear cells that are characterized as cells that look clear when viewed under a microscope.]
obsolete pediatric soft part clear cell sarcoma DOID_4882