Mondo Disease Ontology
6230 terms(s) returned
| Term Type: | Record: 3351 to 3400 of 6230 Records | Page: 68 of 125, First Previous Next Last | Show Records Per Page |
- acute motor and sensory axonal neuropathy
- acute motor axonal neuropathy
- acute mountain sickness
- acute myeloblastic leukemia with maturation
- acute myeloblastic leukemia without maturation
- acute myeloid leukemia
- acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent
- acute myeloid leukemia and myelodysplastic syndromes related to radiation
- acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor
- acute myeloid leukemia by FAB classification
- acute myeloid leukemia with 11q23 abnormalities
- acute myeloid leukemia with BCR-ABL1
- acute myeloid leukemia with CBFA2T3-GLIS2 fusion
- acute myeloid leukemia with CEBPA somatic mutations
- acute myeloid leukemia with FUS-ERG fusion
- acute myeloid leukemia with MNX1-ETV6 fusion
- acute myeloid leukemia with NPM1 somatic mutations
- acute myeloid leukemia with NPM1-MLF1 fusion
- acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
- acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2)
- acute myeloid leukemia with minimal differentiation
- acute myeloid leukemia with multilineage dysplasia
- acute myeloid leukemia with mutated NPM1
- acute myeloid leukemia with t(6;9)(p23;q34)
- acute myeloid leukemia with t(8;16)(p11;p13) translocation
- acute myeloid leukemia with t(8;21)(q22;q22) translocation
- acute myeloid leukemia with t(9;11)(p22;q23)
- acute myeloid leukemia, CEBPA gene mutation
- acute myeloid leukemia, FLT3 internal tandem duplication
- acute myeloid leukemia, FLT3 tyrosine kinase domain point mutation
- acute myeloid leukemia, GATA1 gene mutation
- acute myeloid leukemia, KIT exon 17 mutation
- acute myeloid leukemia, KIT exon 8 mutation
- acute myeloid leukemia, KIT gene mutation
- acute myeloid leukemia, KRAS gene mutation
- acute myeloid leukemia, MLL gene rearrangement
- acute myeloid leukemia, Monosomy 5
- acute myeloid leukemia, Monosomy 7
- acute myeloid leukemia, NRAS gene mutation
- acute myeloid leukemia, Non-KMT2A MLLT10 rearrangement positive
- acute myeloid leukemia, PTPN11 gene mutation
- acute myeloid leukemia, RUNX1 gene mutation
- acute myeloid leukemia, Trisomy 8
- acute myeloid leukemia, WT1 gene mutation
- acute myeloid leukemia, biallelic CEBPA gene mutation
- acute myeloid leukemia, del(13q14-q21)
- acute myeloid leukemia, del(5q31-q32)
- acute myeloid leukemia, der12p
- acute myeloid leukemia, inv(16)(p13.1;q22)
- acute myeloid leukemia, inv(16)(p13.3;q24.3)
