All terms in DOID

Label Id Description
Teebi hypertelorism syndrome DOID_0081073 [A syndrome characterized by hypertelorism, prominent forehead, thick eyebrows, and short nose with broad and depressed features.]
Teebi hypertelorism syndrome 2 DOID_0081074 [A Teebi hypertelorism syndrome that has_material_basis_in mutation in heterozygous mutation in the CDH11 gene on chromosome 16q21.]
Ziziphus mauritiana NCBITaxon_157914
Ziziphus NCBITaxon_72171
obsolete posttransplantation lymphoproliferative disease DOID_3836
obsolete benign lymphoproliferative disease DOID_3837
obsolete skin lymphoproliferative disease DOID_3838
Takayasu's arteritis DOID_2508 [A vasculitis that involves inflammation of the aorta that carries blood from the heart to the rest of the body.]
Cucurbitales NCBITaxon_71239
fabids NCBITaxon_91835
acute myeloid leukemia with t(6;9) (p23;q34.1) DOID_0081080 [An acute myeloid leukemia associated with t(6;9)(p23;q34), resulting in DEK-NUP214(CAN) fusion protein expression. It is often associated with multilineage dysplasia and basophilia.]
acute promyelocytic leukemia with PML-RARA DOID_0081081 [An acute promyelocytic leukemia that is characterized by a severe coagulopathy and the t(15;17)(q24;q21), generating a PML-RARA fusion gene, and where abnormal promyelocytes predominate.]
acute promyelocytic leukemia DOID_0060318 [An acute myeloid leukemia characterized by accumulation of promyelocytes in the bone marrow and by a translocation between chromosomes 15 and 17.]
acute myeloid leukemia without maturation DOID_0081086 [An acute myeloid leukemia that is characterized by blasts without evidence of significant maturation in the neutrophilic lineage.]
acute myeloid leukemia with maturation DOID_0081087 [An acute myeloid leukemia characterized by blasts with evidence of significant maturation in the neutrophilic lineage.]
chronic myelogenous leukemia, BCR-ABL1 positive DOID_0081088 [A chronic myeloid leukemia that is characterized by an abnormally high number of neutrophils and the expression of the BCR-ABL1 fusion gene.]
acute myeloid leukemia with mutated NPM1 DOID_0081089 [An acute myeloid leukemia with mutation of the nucleophosmin gene. It is usually associated with normal karyotype and frequently has myelomonocytic or monocytic features.]
acute myelomonocytic leukemia DOID_0081082 [An acute myeloid leukemia that is characterized by the proliferation of both neutrophil and monocyte precursors.]
acute myeloid leukemia with inv(3) (q21.3;q26.2) or t(3;3) (q21.3;q26.2) DOID_0081083 [An acute myeloid leukemia associated with inv(3)(q21q26.2) or t(3;3)(q21;q26.2), resulting in the expression of RPN1-EVI1 fusion protein and the reposition of a distal GATA2 enhancer to activate MECOM expression.]
acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) DOID_0081084 [An acute myeloid leukemia that is characterized by the presence of abnormal bone marrow eosinophils and the characteristic cytogenetic abnormality inv(16)(p13.1q22) or t(16;16)(p13.1;q22), which results in the expression of the fusion protein CBFB-MYH11.]