All terms in DOID

Label Id Description
obsolete certain conditions originating in the perinatal period DOID_425
stomach carcinoma in situ DOID_9138 [An in situ carcinoma that is located_in the stomach.]
Joubert syndrome 4 DOID_0110999 [A Joubert syndrome that has_material_basis_in deletions of the NPHP1 gene on chromosome 2q13.]
pulmonary immaturity DOID_424 [A lung disease that is characterized by pulmonary collapse, accompanied by hypoventilation which can affect a lobe, segment, or all of the lung, resulting in a decrease in the ventilation/perfusion ratio.]
seasonal affective disorder DOID_0060167 [A mental depression that involves presentation of depressive symptoms only during a specific season of the year.]
bipolar ll disorder DOID_0060166 [A bipolar disorder that is characterized by at least one hypomanic episode and at least one major depressive episode; with this disorder, depressive episodes are more frequent and more intense than manic episodes.]
Kleine-Levin syndrome DOID_0060165 [A recurrent hypersomnia that is characterized by recurring periods of excessive amounts of sleep and altered behavior.]
pain disorder DOID_0060164 [A somatoform disorder that involves chronic pain in one or more areas, and is thought to be caused by psychological stress.]
dentatorubral-pallidoluysian atrophy DOID_0060162 [An autosomal dominant cerebellar ataxia that has_material_basis_in expansion of CAG triplet repeats (glutamine) encoding a polyglutamine tract in the atrophin-1 protein.]
Kennedy's disease DOID_0060161 [A spinal muscular dystrophy that has_material_basis_in an X-linked recessive expansion of CAG triplet repeats (glutamine) in exon 1 of AR gene encoding the androgen receptor.]
persistent Mullerian duct syndrome DOID_0050791 [A pseudohermaphroditism that is characterized by the persistence of Mullerian duct derivatives (i.e. uterus, cervix, fallopian tubes and upper two thirds of vagina) in a phenotypically and karyotypically male.]
fibular hypoplasia and complex brachydactyly DOID_0050790 [An acromesomelic dysplasia that is characterized by severe reduction or absence of the fibula and complex brachydactyly.]
short QT syndrome DOID_0050793 [A heart conduction disease that is characterized by heart arrhythmia defined as a short QT interval on an EKG (less than 300 ms) that does not significantly change with heart rate, tall and peaked T waves, and a structurally normal heart.]
multiple cutaneous and mucosal venous malformations DOID_0050792 [A vein disease that is characterized by multiple bluish cutaneous or mucosal venous lesions that has_material_basis_in heterozygous mutation in the TEK gene on chromosome 9p21.]
maternally_imprinted SO_0000135
sequence_attribute SO_0000400
spindle cell hemangioma DOID_496
obsolete mycosis fungoides involving intrapelvic lymph nodes DOID_9105
steroid CHEBI_35341
obsolete carcinoma in situ of male genital organs DOID_9103