All terms in DOID

Label Id Description
penis carcinoma in situ DOID_8872 [An in situ carcinoma that is located_in the penis.]
penile disease DOID_1529
otitis SYMP_0000873 [Otitis is a ear symptom characterized as a general term for inflammation or infection of the ear, in both humans and other animals.]
hematoma SYMP_0000874 [A skin and integumentary tissue symptom that is characterized by a mass of usually clotted blood that forms in a tissue, organ, or body space as a result of a broken blood vessel generally the result of hemorrhage, or more specifically, internal bleeding.]
icteric mucous membrane SYMP_0000871 [A skin and integumentary tissue symptom that is characterized by yellowed mucous membranes due to bile or bilirubin accumulation.]
obsolete X-linked dominant disease DOID_0080340
icteric skin SYMP_0000872 [A skin and integumentary tissue symptom that is characterized by yellowed skin due to bile or bilirubin accumulation.]
obsolete herpetic vulvovaginitis DOID_8876 [A genital herpes that results_in infection located_in vulva and located_in vagina, has_material_basis_in Human herpesvirus 1 or Human herpesvirus 2 and has_symptom fever, has_symptom lymphadenopathy, and has_symptom lesions.]
obsolete X-linked recessive disease DOID_0080341
icteric eyes SYMP_0000870 [Icteric eyes is a eye symptom characterized by yellowed eyes due to bile or bilirubin accumulation.]
ceruminoma DOID_7549
mitochondrial complex IV deficiency nuclear type 2 DOID_0080357 [A COX deficiency, infantile mitochondrial myopathy that has_material_basis_in compound heterozygous mutation in the SCO2 gene on chromosome 22q13.]
mitochondrial complex IV deficiency nuclear type 6 DOID_0080358 [A COX deficiency, infantile mitochondrial myopathy that has_material_basis_in compound heterozygous mutation in the COX15 gene on chromosome 10q24.]
Rhipicephalus pumilio NCBITaxon_127007
mitochondrial complex IV deficiency nuclear type 9 DOID_0080359 [A COX deficiency, infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COA5 gene on chromosome 2q11.]
osteoarthritis susceptibility 5 MIM_612400
osteoarthritis susceptibility 6 MIM_612401
continuous fever SYMP_0000888 [A fever that is characterized by a temperature remaining above normal throughout the day and which does not fluctuate more than 1 degree Celsius in 24 hours.]
X-linked recessive hypophosphatemic rickets DOID_0080353 [A rickets that has_material_basis_in mutation in the CLCN5 gene on chromosome Xp11.22.]
rickets DOID_10609 [A bone remodeling disease that has_material_basis_in impaired mineralization or calcification of bones before epiphyseal closure due to deficiency or impaired metabolism of vitamin D, phosphorus or calcium which results_in softening and deformity located_in bone.]