All terms in DOID

Label Id Description
cerebral angioma DOID_6621 [A brain angioma that is characterized by vascular abnormalities that develops from cranial and spinal blood vasculature, has_material_basis_in abnormally proliferating cells, derives_from endothelial cells in and about the vascular lumen.]
nipple duct carcinoma DOID_7953 [A nipple carcinoma that is located_in the nipple duct.]
sarcomatoid penile squamous cell carcinoma DOID_7958
cervical adenoma malignum DOID_6627 [A cervical mucinous adenocarcinoma that is well differentiated, consisting of an endocervical glandular hyperplasia of lobular architecture resembling glands but with the characteristics of adenocarcinoma.]
obsolete malignant neoplasm of nipple DOID_6628
duodenal gastrinoma DOID_7959
obsolete EBV-related posttransplantation lymphoproliferative disease DOID_7956 [An Epstein-Barr virus related lymphoma and is_a posttransplantation lymphoproliferative disorder that derives_from lymphocytes after organ transplant, has_material_basis_in Human herpesvirus 4.]
autoimmune disease of skin and connective tissue DOID_0060039 [An autoimmune disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the skin and connective tissue.]
bullous skin disease DOID_8502 [A dermatitis that is characterized by blisters filled with a watery fluid, located_in skin. The disease is associated with the amount of gluten ingested.]
appendage blood vessel UBERON_0007301
intracranial meningioma DOID_0080842 [A meningioma that arises within the cranial cavity.]
malignant type A thymoma DOID_7927
supratentorial meningioma DOID_0080843 [A meningioma that affects the supratentorial brain.]
testis refractory cancer DOID_7928
omodysplasia 1 DOID_0080844 [An omodysplasia that is characterized by severe congenital micromelia with shortening and distal tapering of the humeri and femora to give a club-like appearance and that has_material_basis_in homozygous or compound heterozygous mutation in the GPC6 gene on chromosome 13q32.]
omodysplasia DOID_0060288 [An osteochondrodysplasia that is characterized by severe limb shortening and facial dysmorphism.]
optic atrophy 12 DOID_0080840 [An optic atrophy that is characterized by slowly progressive visual impairment with onset usually in the first decade and that has_material_basis_in heterozygous mutation in the AFG3L2 gene on chromosome 18p11.]
ocular motor apraxia, Cogan type DOID_0080849 [An eye disease that is characterized by defective or absent horizontal voluntary eye movements, and defective or absent horizontal ocular attraction movements.]
omodysplasia 2 DOID_0080845 [An omodysplasia that is characterized by shortened humeri, dislocated radial heads, shortened first metacarpals, craniofacial dysmorphism, and variable genitourinary anomalies and that has_material_basis_in heterozygous mutation in the FZD2 gene on chromosome 17q21.]
latent autoimmune diabetes in adults DOID_0080846 [A type 1 diabetes mellitus that is characterized by a less intensive autoimmune process, highly variable β-cell destruction, different degrees of insulin resistance and heterogeneous titre and pattern of islet autoantibody, sharing features with both type 1 and type 2 diabetes mellitus.]