All terms in DOID

Label Id Description
myeloid neoplasm DOID_0070004 [A bone marrow cancer that is formed of any one of the bone marrow cells belonging to the granulocytic (neutrophil, eosinophil, basophil), monocytic/macrophage, erythroid, megakaryocytic and mast cell lineages.]
bone marrow cancer DOID_4960 [A hematopoietic cancer that derives_from the blood-forming stem cells of the bone marrow.]
cerebral cavernous malformation 2 DOID_0060670 [A cerebral cavernous malformation that has_material_basis_in mutation in the CCM2 gene on chromosome 7p13.]
cerebral cavernous malformation DOID_0060669 [A cerebrovascular disease that is characterized by dilated blood-filled capillaries lacking structural support.]
epiphysis UBERON_0001437
zone of long bone UBERON_0005055
Seckel syndrome 9 DOID_0070005 [A Seckel syndrome that has_material_basis_in homozygous mutation in the TRAIP gene on chromosome 3p21.]
cerebral cavernous malformation 3 DOID_0060671 [A cerebral cavernous malformation that has_material_basis_in mutation in the PDCD10 gene on chromosome 3q26.1.]
metaphysis UBERON_0001438
3-methylglutaconic aciduria type 9 DOID_0070002 [A 3-methylglutaconic aciduria that has_material_basis_in homozygous mutation in the TIMM50 gene on chromosome 19q13.]
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions DOID_0060672 [A frontotemporal dementia characterized by variable phenotypic expression typically including social, behavioral, or language deterioration, rather than memory or motor deficits and the presence of TARDBP-positive inclusions that has_material_basis_in mutation in the GRN gene on chromosome 17q21.31.]
frontotemporal dementia DOID_9255 [A dementia characterized by progressive neuronal loss predominantly involving the frontal and/or temporal lobes of the brain resulting in a gradual and progressive decline in behavior or language.]
blastoma DOID_0070003 [A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from precursor cells called blast cells.]
Peters anomaly DOID_0060673 [A corneal disease characterized by a central corneal leukoma and absence of the posterior corneal stroma and Descemet membrane that has_material_basis_in mutation in the PAX6 gene on chromosome 11p13, the PITX2 gene on chromosome 4q25, the CYP1B1 gene on chromosome 2p22.2, or the FOXC1 gene on chromosome 6p25.3.]
Abnormal muscle physiology HP_0011804
buccal salivary gland UBERON_0012102
saliva-secreting gland UBERON_0001044
Mansoniini NCBITaxon_254792
Culicinae NCBITaxon_43817
neuron projection bundle UBERON_0000122