All terms in DOID

Label Id Description
Bartholin's gland cancer DOID_60003 [A vulva cancer that is located in Bartholin's gland.]
benign vascular tumor DOID_60006
susceptibility to dyslexia 3 MIM_604254
cod food product FOODON_00001750
fish food product FOODON_00001248
obsolete idiopathic generalized epilepsy 5 DOID_0111320 [An idiopathic generalized epilepsy that has_material_basis_in variation in a region on chromosome 10p11.22.]
juvenile myoclonic epilepsy 4 DOID_0111327 [A juvenile myoclonic epilepsy that has_material_basis_in variation in a region on chromosome 5q12-q14.]
juvenile myoclonic epilepsy 9 DOID_0111328 [A juvenile myoclonic epilepsy that has_material_basis_in heterozygous variation in a region on chromosome 2q33-q36.]
juvenile myoclonic epilepsy 10 DOID_0111325 [A juvenile myoclonic epilepsy that has_material_basis_in heterozygous mutation in ICK on chromosome 6p12.1.]
juvenile myoclonic epilepsy 3 DOID_0111326 [A juvenile myoclonic epilepsy that has_material_basis_in variation in a region on chromosome 6p21.]
obsolete idiopathic generalized epilepsy 9 DOID_0111323 [An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the CACNB4 on chromosome 2q23.3.]
juvenile absence epilepsy 1 DOID_0111324 [A juvenile absence epilepsy that has_material_basis_in heterozygous mutation in EFHC1 on 6p12.2.]
juvenile absence epilepsy DOID_0060172 [An adolescence-adult electroclinical syndrome statring between the age of ten to 17 years characterized by the occurrence of typical absence seizures.]
obsolete idiopathic generalized epilepsy 7 DOID_0111321 [An idiopathic generalized epilepsy that has_material_basis_in variation in a region on chromosome 15q14.]
obsolete idiopathic generalized epilepsy 8 DOID_0111322 [An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the CASR on chromosome 3q13.3-q21.1.]
Geotrichum NCBITaxon_43987
pyridoxamine 5'-phosphate oxidase deficiency DOID_0111329 [A vitamin metabolic disorder characterized by vitamin B6 deficienc resulting in neonatal-onset of severe seizures that can be controlled with pyridoxal 5'-phosphate treatment that has_material_basis_in homozygous or compound heterozygous mutation in PNPO on 17q21.32.]
organic univalent group CHEBI_51447
organic group CHEBI_33247
Erysipelothrix rhusiopathiae NCBITaxon_1648