All terms in DOID

Label Id Description
exocervical carcinoma DOID_2892 [A cervix carcinoma that is located_in the exocervix.]
Theropoda NCBITaxon_436491
Saurischia NCBITaxon_436489
obsolete commensal streptococcal infectious disease DOID_2898
immunodeficiency 90 DOID_0061060 [A primary immunodeficiency disease that is characterized by infancy or early childhood with recurrent fevers and bacterial or viral infections associated with central nervous system symptoms, including irritability, drowsiness, variable seizures, and white matter abnormalities on brain imaging and that has_material_basis_in homozygous or compound heterozygous mutation in the FADD gene on chromosome 11q13.]
mechanical ectropion DOID_1569
immunodeficiency 91 DOID_0061061 [A primary immunodeficiency disease that is characterized by both immunodeficiency and recurrent infections, often to viruses or mycobacteria, as well as by hyperinflammation with systemic involvement and that has_material_basis_in homozygous or compound heterozygous mutation in the ZNFX1 gene on chromosome 20q13.]
pulmonary systemic sclerosis DOID_1578
innate lymphoid cell CL_0001065
limited scleroderma DOID_1577
rheumatic disease DOID_1575 [A musculoskeletal system disease that involves inflammation or pain in the muscles, joints, or fibrous tissue.]
alcohol use disorder DOID_1574 [A substance abuse that involves the recurring use of alcoholic beverages despite negative consequences.]
Myodes glareolus NCBITaxon_447135
Myodes NCBITaxon_447134
communicating hydrocephalus DOID_1573
normal pressure hydrocephalus DOID_1572
spastic ectropion DOID_1571
immunodeficiency 89 DOID_0061059 [A primary immunodeficiency disease that is characterized by adult onset of recurrent infections, allergies, microcytic anemia, and Crohn disease and that has_material_basis_in homozygous mutation in the CARD10 gene on chromosome 22q13.]
malignant cell CL_0001064
neoplastic cell CL_0001063