All terms in DOID

Label Id Description
Dibothriocephalus latus NCBITaxon_60516
Dibothriocephalus NCBITaxon_2267273
ceftazidime CHEBI_3508
cataract DOID_83 [A lens disease characterized by clouding of the lens inside the eye which leads to a decrease in vision.]
lens disease DOID_110 [An eye disease that affects the lens of the eye, which is the transparent disc that focuses light to the photosensors in the back of the eye.]
osteochondritis dissecans DOID_84 [An ischemic bone disease that results_in necrosis located_in epiphysis.]
ischemic bone disease DOID_0080008 [A bone disease that results_in an interruption of blood supply located_in bone.]
myotonic cataract DOID_82 [A cataract that is characterized by multicolored, iridescent opacification of the lens of the eye, and associated with myotonic dystrophy.]
dill allergy DOID_0081006 [A food allergy triggered by dill (Anethum graveolens).]
vegetable allergy DOID_0070334 [A food allergy triggered by a vegetable food product.]
nocturnal enuresis SYMP_0000606 [A urinary incontinence that is characterized by involuntary urination at night in children five years of age or older.]
urinary incontinence SYMP_0000492 [A urinary system symptom that is characterized by the an inability of the body to control the evacuative functions.]
RNASET2-deficient cystic leukoencephalopathy DOID_0081007 [A leukodystrophy that is characterized by non-progressive leukoencephalopathy, bilateral cysts in the anterior part of the temporal lobe, cerebral white matter anomalies and severe psychomotor impairment.]
hallucination SYMP_0000607 [Hallucination is a general symptom where there is a perception of something (as a visual image or a sound) with no external cause usually arising from a disorder of the nervous system (as in delirium tremens or in functional psychosis without known neurological disease) or in response to drugs (as LSD).]
intellectual developmental disorder with cardiac arrhythmia DOID_0081008 [A syndrome that is characterized by delayed psychomotor development, severe intellectual disability with poor or absent speech, and bradycardia and/or cardiac sinus arrhythmias and that has_material_basis_in homozygous or compound heterozygous mutation in the GNB5 gene on chromosome 15q21.]
wheezing SYMP_0000604 [An abnormal chest sound that is characterized by breathing with difficulty usually with a whistling sound.]
carbocyclic compound CHEBI_33598
organic cyclic compound CHEBI_33832
homocyclic compound CHEBI_33597
Bardet-Biedl syndrome 20 DOID_0081009 [A Bardet-Biedl syndrome that is characterized by rod-cone dystrophy, postaxial polydactyly, truncal obesity, renal anomalies, and learning disability, as well as hypogonadism in males and genital abnormalities in females and that has_material_basis_in homozygous mutation in the IFT172 gene on chromosome 2p23.]