Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
pyelitis	DOID_2744
obsolete axillary cancer	DOID_5097
Omsk hemorrhagic fever virus	NCBITaxon_12542
Flavivirus	NCBITaxon_11051
obsolete syphilitic disseminated chorioretinitis	DOID_11409
obsolete bronchial tuberculosis	DOID_12739	[A pulmonary tuberculosis which involves inflammation of bronchi resulting in irregular circumferential bronchial wall thickening that leads to narrowed or even obstructed airways.]
gas molecular entity	CHEBI_138675	[Any main group molecular entity that is gaseous at standard temperature and pressure (STP; 0degreeC and 100 kPa).]
choroiditis	DOID_11406
choroid disease	DOID_1417
diphtheria	DOID_11405	[A primary bacterial infectious disease that is characterized by sore throat, low fever, and an adherent membrane (a pseudomembrane) on the tonsils, pharynx, and/or nasal cavity. A milder form of diphtheria can be restricted to the skin. It is caused by Corynebacterium diphtheriae, an aerobic Gram-positive bacterium. Diphtheria toxin spreads through the bloodstream and can lead to potentially life-threatening complications that affect other organs of the body, such as the heart and kidneys.]
Corynebacterium diphtheriae	NCBITaxon_1717
Neu-Laxova syndrome 2	DOID_0080075	[A serine deficiency that is characterized by multiple fatal malformations including ichthyosis, microcephaly, central nervous system abnormalities, limb deformities, intrauterine growth restriction, proptosis, anasarca, and micrognathia, and has_material_basis_in autosomal recessive inheritance of mutation in the PSAT1 gene on chromosome 9q21.1, causing issues producing the amino acid serine.]
serine deficiency	DOID_0050721	[An amino acid metabolic disorder that has_material_basis_in defects in the biosynthesis of the amino acid L-serine.]
Neu-Laxova syndrome 1	DOID_0080076	[A serine deficiency that is characterized by multiple fatal malformations including ichthyosis, microcephaly, central nervous system abnormalities, limb deformities, intrauterine growth restriction, proptosis, anasarca, and micrognathia, and has_material_basis_in autosomal recessive inheritance of mutation in the PHGDH gene on chromosome 1p12, causing issues producing the amino acid serine.]
hypophosphatemic nephrolithiasis/osteoporosis 1	DOID_0080077
inclusion-cell disease	DOID_0080070
pseudo-Hurler polydystrophy	DOID_0080071
neuronal intestinal dysplasia	DOID_0080072
spina bifida occulta	DOID_0080073
acromesomelic dysplasia	DOID_0080049	[An osteochondrodysplasia that has_material_basis_in mesomelia and acromelia, which results_in short limb dwarfism.]