All terms in DOID

Label Id Description
obsolete glaucoma associated with tumors or cysts DOID_9899
visceral striated muscle tissue UBERON_8600006
visceral muscle tissue UBERON_8600004
striated muscle tissue UBERON_0002036
muscle tissue UBERON_0002385
vitiligo DOID_12306 [An autoimmune disease that causes depigmentation of patches of skin resulting from loss of function or death of melanoctyes.]
congenital hypoplastic anemia DOID_1342 [An aplastic anemia that is characterized by insufficient production of red blood cells, usually seen in the first year of life.]
Bloch-Sulzberger syndrome DOID_12305
conjunctival pigmentation DOID_12304
obsolete diphtheritic membranous angina DOID_12302 [A diphtheria that involves a bluish white membrane formation on the faucial pillars, uvula, soft palate and tonsils.]
obsolete speckled lentiginous nevus DOID_12301
miliary tuberculosis DOID_9861 [An extrapulmonary tuberculosis that results in formation of tiny lesions in all the organs.]
obsolete toxic gastroenteritis and colitis DOID_8530
intermediate malignant teratoma DOID_7202 [A malignant teratoma characterized by the presence of an intermediate amount of undifferentiated tissues.]
urticaria pigmentosa DOID_12309
gastroesophageal reflux disease DOID_8534
Dubin-Johnson syndrome DOID_12308 [A bilirubin metabolic disorder that involves elevated levels of unconjugated bilirubin without elevation of liver alanine transaminase and aspartate transaminase enzymes as a result of the deficient ability of hepatocytes to secrete conjugated bilirubin into the bile.]
anterior corneal pigmentation DOID_12307
melanomatosis DOID_7206
hereditary fructose intolerance syndrome DOID_9869 [A carbohydrate metabolic disorder characterized by recurrent vomiting, abdominal pain, and hypoglycemia that may be fatal after introduction of fructose or sucrose to the diet that has_material_basis_in homozygous or compound heterozygous mutation in the aldolase B gene (ALDOB) on chromosome 9q31.]