All terms in DOID

Label Id Description
obsolete specific bursitis often of occupational origin DOID_12223
Bunostominae NCBITaxon_53477
histiocytosis-lymphadenopathy plus syndrome DOID_0111278 [A syndrome characterized by histiocytosis, hyperpigmentation, hypertrichosis, hepatosplenomegaly, heart anomalies, hearing loss, hypogonadism, and reduced height that has_material_basis_in homozygous or compound heterozygous mutation in SLC29A3 on 10q22.1. This syndrome comprises features from 4 histiocytic disorders that were previously considered distinct: Faisalabad histiocytosis, sinus histiocytosis with massive lymphadenopathy, H syndrome, and pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome.]
choroideremia DOID_9821
central gyrate choroidal dystrophy DOID_9820
partial central choroid dystrophy DOID_9822
susceptibility to psoriasis 5 MIM_604316
obsolete total or subtotal old retinal detachment DOID_9824
obsolete Partial recent retinal detachment with retinal dialysis DOID_9823
obsolete drug abstinence syndrome or symptom DOID_9829
neonatal abstinence syndrome DOID_9828 [A withdrawal disorder that is characterized by a group of problems that occur in a newborn who was exposed to addictive illegal or prescription drugs while in the mother's womb or postnatally following the discontinuance of drug treatment.]
withdrawal disorder DOID_0060001 [A substance-related disorder that occurs upon the abrupt discontinuation/separation or a decrease in dosage of the intake of medications, recreational drugs, and alcohol.]
susceptibility to idiopathic generalized epilepsy 2 MIM_606972
radioulnar synostosis DOID_9827
Ruijs-Aalfs syndrome DOID_0111264 [A syndrome characterized by genomic instability and susceptibility toward early onset hepatocellular carcinoma that has_material_basis_in homozygous or compound heterozygous mutation in SPRTN on 1q42.2.]
obsolete glaucoma associated with pupillary block DOID_13562
Boucher-Neuhauser syndrome DOID_0111265 [A syndrome characterized by spinocerebellar ataxia, hypogonadotropic hypogonadism, and chorioretinal dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in PNPLA6 on 19p13.2.]
optic disk drusen DOID_13561
infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly DOID_0111262 [A brain disease characterized by cerebral and cerebellar atrophy, postnatal progressive microcephaly and intellectual disability that has_material_basis_in homozygous or compound heterozygous mutation in MED17 on 11q21.]
subserous uterine fibroid DOID_13560 [An uterine fibroid that is located adjacent to the outside of the uterus.]