All terms in DOID

Label Id Description
bullous pemphigoid DOID_8506 [A pemphigoid that is characterized by large blisters.]
juvenile dermatitis herpetiformis DOID_8507
hypertropia DOID_9837
cortical senile cataract DOID_13574 [A senile cataract that is characterized by opacification of the lens cortex, caused by dehydration of lens fibers, and is related to aging.]
obsolete schizo-affective type schizophrenia chronic state with acute exacerbation DOID_13573
familial febrile seizures 8 DOID_0111298 [A familial febrile seizures that has_material_basis_in heterozygous mutation in the GABRG2 gene on chromosome 5q34.]
hypersensitivity reaction type III disease DOID_1557 [A hypersensitivity reaction disease that is characterized by the accumulation of antigen-antibody immune complexes, causing an inflammatory response and injury.]
generalized epilepsy with febrile seizures plus 7 DOID_0111295 [A generalized epilepsy with febrile seizures plus that has_material_basis_in heterozygous mutation in SCN9A on chromosome 2q24.3.]
generalized epilepsy with febrile seizures plus 10 DOID_0111296 [A generalized epilepsy with febrile seizures plus that has_material_basis_in heterozygous mutation in HCN1 on chromosome 5p12.]
generalized epilepsy with febrile seizures plus 4 DOID_0111293 [A generalized epilepsy with febrile seizures plus that has_material_basis_in variation in a region on chromosome 2p24.]
generalized epilepsy with febrile seizures plus 2 DOID_0111294 [A generalized epilepsy with febrile seizures plus that has_material_basis_in heterozygous mutation in SCN1A on chromosome 2q24.3.]
psoriasis 12 DOID_0111291 [A psoriasis that has_material_basis_in variation in a region on chromosome 20q13 that includes RNF114.]
obsolete idiopathic generalized epilepsy 10 DOID_0111292 [An idiopathic generalized epilepsy that has_material_basis_in variation in the GABRD on chromosome 1p36.33.]
kwashiorkor DOID_13579 [A protein-energy malnutrition that is characterized by severe lack of protein and edema or anasarca, has_symptom swelling, gastrointestinal upset, dehydration, thin dry skin, and cough, and has_material_basis_in severe deficit of protein, resulting in lack of albumin causing decreased oncotic pressure in the vasculature and increased activation of the renin-angiotensin axis and antidiuretic hormone.]
obsolete ascorbic acid deficiency DOID_13577
histoplasmosis meningitis DOID_12246
twin-to-twin transfusion syndrome DOID_13576 [A neonatal anemia that is characterized by an increased number of arteriovenous anastomoses deep in the placenta. These capillary connections occur in the cotyledon portion of the placenta. Unidirectional flow can occur in these arteriovenous anastomoses and result in shunting of blood towards one twin and away from the other when the arteriovenous anastomoses are unbalanced.]
neonatal anemia DOID_11244 [An anemia that is characterized by a lower red blood cell count than normal in neonates.]
obsolete histoplasmosis endocarditis DOID_12245 [A histoplasmosis endocarditis that results_in inflammation located_in endocardium, has_material_basis_in Histoplasma capsulatum var duboisii or has_material_basis_in Histoplasma capsulatum var capsulatum, transmitted_by airborne spores and has_symptom murmurs, has_symptom peripheral edema, has_symptom pulmonary rales, has_symptom petechia and has_symptom skin lesions.]
generalized epilepsy with febrile seizures plus 8 DOID_0111299 [A generalized epilepsy with febrile seizures plus that has_material_basis_in variation in a region on chromosome 6q16.3-q22.31.]