All terms in DOID

Label Id Description
gliofibroma DOID_4856
laryngeal adenoid cystic carcinoma DOID_4869
laryngeal carcinoma DOID_2600 [A larynx cancer that has_material_basis_in epithelial cells.]
genic_downstream_transcript_variant SO_0002152
gene_variant SO_0001564
genic_upstream_transcript_variant SO_0002153
brain stem astrocytic neoplasm DOID_4860 [A brain stem glioma that is characterized by mass lesion of the brainstem, associated cranial nerve nuclei and long tracts, has_material_basis_in abnormally proliferating cells derives_from astrocytes.]
brain stem glioma DOID_4202 [A brain stem cancer that is characterized by mass lesion of the brainstem, associated cranial nerve nuclei and long tracts, has_material_basis_in abnormally proliferating cells, derives_from glial cells.]
chronic wasting disease DOID_3530
prion disease DOID_649 [A brain disease that is characterized by brain damage resulting from the abnormal folding, clumping and accumulation of cellular proteins in the brain induced by prion proteins.]
obsolete peste des petits ruminants infectious disease DOID_3532 [A viral infectious disease that results_in infection in ruminants, has_material_basis_in Peste-des-petits-ruminants virus, which is transmitted_by contact with oronasal and ocular secretions, urine, and feces. The infection results_in_formation_of lesions on the gums, lips and palate.]
obsolete Rubella virus infectious disease DOID_4864 [A viral infectious disease that results_in infection, has_material_basis_in Rubella virus, which is transmitted_by direct contact with the infected person through coughing and sneezing, and transmitted_by congenital method.]
spinal cord astrocytoma DOID_4863
obsolete Morbillivirus infectious disease DOID_3533 [A Paramyxoviridae infectious disease that results_in infection in dogs, seals, cattle and humans, has_material_basis_in Morbillivirus.]
Lafora disease DOID_3534 [A progressive myoclonus epilepsy characterized by myoclonus and/or generalized seizures, visual hallucinations, and progressive neurological decline with onset between 8 and 18 years of age that has_material_basis_in homozygous or compound heterozygous mutation in either NHLRC1 on chromosome 6p22.3 or EPM2A on chromosome 6q24.3.]
progressive myoclonus epilepsy DOID_891 [A variable age at onset electroclinical syndrome characterized by a relentlessly progressive disease course until death.]
salivary gland adenoid cystic carcinoma DOID_4866 [A salivary gland carcinoma that is characterized by a distinctive pattern in which abnormal nests or cords of epithelial cells surround and/or infiltrate ducts or glandular structures within the affected organ. These structures are typically filled with a mucous-like material or contain abnormal fibrous membranes.]
obsolete Togaviridae infectious disease DOID_4865 [A (+)ssRNA virus infectious disease that results_in infection in animals and humans, has_material_basis_in Togaviridae viruses.]
Unverricht-Lundborg syndrome DOID_3535 [A progressive myoclonus epilepsy characterized by onset between 6 and 13 years of age of action- and stimulus-sensitive myoclonus, tonic-clonic seizures with ataxia, and a mild cognitive decline.]
prostate adenoid cystic carcinoma DOID_4868