All terms in DOID

Label Id Description
obsolete tuberculous myelitis DOID_10173
primary mediastinal B-cell lymphoma DOID_0080210 [A large B-cell lymphoma that is is characterized by a diffuse proliferation of medium to large B-cells associated with sclerosis.]
nodal marginal zone lymphoma DOID_0080211 [A marginal zone B-cell lymphoma which morphologically resembles lymph nodes involved by marginal zone lymphomas of extranodal or splenic types, but without evidence of extranodal or splenic disease.]
marginal zone lymphoma DOID_0050748 [A B-cell lymphoma arising from the marginal zone of lymphoid tissues that is characterized by the presence of small to medium sized atypical lymphocytes.]
organic halide salt CHEBI_51069
organic salt CHEBI_24868
polycystic kidney disease 4 DOID_0080212 [A autosomal recessive polycystic kidney disease that has_material_basis_in mutation in the PKD4 gene.]
autosomal recessive polycystic kidney disease DOID_0110861 [A polycystic kidney disease characterized by the presence of multiple cysts located_in the kidney resulting from ciliopathy that disrupts the function of primary cilium, inherited in an autosomal recessive fashion.]
punctate palmoplantar keratoderma type II DOID_0080213 [A punctate palmoplantar keratoderma that is characterized by multiple, asymptomatic, 1 to 2 mm-long, firm, hyperkeratotic projections on the palms, soles and digits.]
primary spontaneous pneumothorax DOID_0080218 [A pneumothorax that is characterized by an abnormal accumulation of air in the space between the lungs and the chest cavity that can result in the partial or complete collapse of a lung.]
pneumothorax DOID_1673 [A pleural disease that is characterized as an abnormal collection of air in the pleural space between the lung and the chest wall.]
dystransthyretinemic hyperthyroxinemia DOID_0080219 [A hyperthyroxinemia that is characterized by an increased affinity for thyroxine (T4) by transthyretin in clinically euthyroid individuals and that has_material_basis_in heterozygous mutation in the TTR gene on chromosome 18q12.]
hyperthyroxinemia DOID_2855 [A thyroid gland disease that is characterized by elevated thyroxine levels in the blood.]
neuroretinitis DOID_10176 [An eye disease that is characterized by inflammation of the retina.]
malignant hypertensive renal disease DOID_10177
Vascular skin abnormality HP_0011276
Generalized abnormality of skin HP_0011354
nutrition disease DOID_374 [An acquired metabolic disease that is characterized by an insufficient intake of food or of certain nutrients, by an inability of the body to absorb and use nutrients, or by overconsumption of certain foods.]
copper deficiency myelopathy DOID_5112 [A nutritional deficiency disease that is characterized by deficiency of copper, causing spastic gait and ataxia, often with anemia and neutropenia, has_symptom imbalance and jerking movements, and has_material_basis_in copper deficiency possibly due to malabsorption or excess zinc ingestion.]
obsolete ceruminous tumor DOID_6447