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Every indexed disease entity from the canonical taxonomy. Counters aggregate over each entity's descendants; completeness dots show which data domains hold at least one record.
9,510 entities
| Cancer | Type | Parent(s) | Active trials (count) | Publications 5y (count) | Evidence items (count) | Children | Completeness | Data confidence |
|---|---|---|---|---|---|---|---|---|
| Acute Myeloid Leukemia without MaturationCI-CAN-00007139Hematologic | Hematologic Malignancy | Acute Myeloid Leukemia, Not Otherwise Specified | 2 | 7 | 0 | 2 | Low confidence | |
| Acute Myeloid Leukemia with RAM ImmunophenotypeCI-CAN-00007138HematologicPediatric | Hematologic Malignancy | Childhood Acute Myeloid Leukemia | 0 | 0 | 0 | 0 |
| Insufficient data |
| Acute Myeloid Leukemia with RUNX1 MutationCI-CAN-00008670Hematologic | Molecular Subtype | Acute Myeloid Leukemia with Myelodysplasia-Related Gene Mutations, AML with Recurrent Genetic Abnormalities | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with SF3B1 MutationCI-CAN-00008671Hematologic | Molecular Subtype | Acute Myeloid Leukemia with Myelodysplasia-Related Gene Mutations | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with SRSF2 MutationCI-CAN-00008672Hematologic | Molecular Subtype | Acute Myeloid Leukemia with Myelodysplasia-Related Gene Mutations | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with STAG2 MutationCI-CAN-00008673Hematologic | Molecular Subtype | Acute Myeloid Leukemia with Myelodysplasia-Related Gene Mutations | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with t(10;11)(p12.3;q23.3); MLLT10-KMT2ACI-CAN-00009305Hematologic | Molecular Subtype | Acute Myeloid Leukemia with a Variant KMT2A Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with t(10;11)(q21.3;q23.3); TET1-KMT2ACI-CAN-00009306Hematologic | Molecular Subtype | Acute Myeloid Leukemia with a Variant KMT2A Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with t(11;19)(q23.3;p13.1); KMT2A-ELLCI-CAN-00009307Hematologic | Molecular Subtype | Acute Myeloid Leukemia with a Variant KMT2A Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with t(11;19)(q23.3;p13.3); KMT2A-MLLT1CI-CAN-00009308Hematologic | Molecular Subtype | Acute Myeloid Leukemia with a Variant KMT2A Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with t(16;16)(p13.1;q22); CBFB-MYH11CI-CAN-00009309Hematologic | Molecular Subtype | Acute Myeloid Leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11 | 4 | 0 | 0 | 1 | Low confidence |
| Acute Myeloid Leukemia with t(3;12)(q26.2;p13.2); ETV6-MECOMCI-CAN-00009310Hematologic | Molecular Subtype | Acute Myeloid Leukemia with a Variant MECOM Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with t(3;21)(q26.2;q22.1); MECOM-RUNX1CI-CAN-00009311Hematologic | Molecular Subtype | Acute Myeloid Leukemia with a Variant MECOM Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with t(3;3)(q21.3;q26.2); GATA2, MECOMCI-CAN-00009312Hematologic | Molecular Subtype | Acute Myeloid Leukemia with inv(3)(q21.3;q26.2) or t(3;3)(q21.3;q26.2); GATA2, MECOM | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with t(3;8)(q26.2;q24); MYC, MECOMCI-CAN-00009313Hematologic | Molecular Subtype | Acute Myeloid Leukemia with a Variant MECOM Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with t(4;11)(q21.3;q23.3); AFF1-KMT2ACI-CAN-00009314Hematologic | Molecular Subtype | Acute Myeloid Leukemia with a Variant KMT2A Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with t(6;11)(q27;q23.3); MLLT4-KMT2ACI-CAN-00009315Hematologic | Molecular Subtype | Acute Myeloid Leukemia with a Variant KMT2A Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with t(6;9)(p22.3;q34.1); DEK-NUP214CI-CAN-00008674Hematologic | Molecular Subtype | Acute Myeloid Leukemia with Genetic Abnormalities, AML with Recurrent Genetic Abnormalities | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with t(7;12)(q36;p13); HLXB9-ETV6CI-CAN-00004305HematologicPediatric | Molecular Subtype | Infant Leukemia | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with t(8;16)(p11.2;p13.3); KAT6A-CREBBPCI-CAN-00008675Hematologic | Molecular Subtype | Acute Myeloid Leukemia with Genetic Abnormalities | 0 | 0 | 3 | 2 | Low confidence |
| Acute Myeloid Leukemia with t(8;21)(q22;q22.1); RUNX1-RUNX1T1CI-CAN-00009226Hematologic | Molecular Subtype | AML with Recurrent Genetic Abnormalities, Core Binding Factor Acute Myeloid Leukemia | 4 | 4 | 5 | 2 | Medium confidence |
| Acute Myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2ACI-CAN-00009227Hematologic | Molecular Subtype | Acute Myeloid Leukemia with KMT2A Rearrangement, AML with Recurrent Genetic Abnormalities | 2 | 0 | 0 | 2 | Low confidence |
| Acute Myeloid Leukemia with Trisomy 8CI-CAN-00008676Hematologic | Hematologic Malignancy | Acute Myeloid Leukemia with Myelodysplasia-Related Cytogenetic Abnormalities | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with U2AF1 MutationCI-CAN-00008677Hematologic | Molecular Subtype | Acute Myeloid Leukemia with Myelodysplasia-Related Gene Mutations | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myeloid Leukemia with ZRSR2 MutationCI-CAN-00008678Hematologic | Molecular Subtype | Acute Myeloid Leukemia with Myelodysplasia-Related Gene Mutations | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Myelomonocytic LeukemiaCI-CAN-00007140Hematologic | Hematologic Malignancy | Acute Myeloid Leukemia, Not Otherwise Specified | 3 | 21 | 0 | 4 | Low confidence |
| Acute Myelomonocytic Leukemia with Abnormal EosinophilsCI-CAN-00008679Hematologic | Hematologic Malignancy | Acute Myelomonocytic Leukemia | 0 | 8 | 0 | 0 | Low confidence |
| Acute Myelomonocytic Leukemia without Abnormal EosinophilsCI-CAN-00008680Hematologic | Hematologic Malignancy | Acute Myelomonocytic Leukemia | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Panmyelosis with MyelofibrosisCI-CAN-00007141Hematologic | Hematologic Malignancy | Acute Myeloid Leukemia, Not Otherwise Specified | 0 | 15 | 0 | 0 | Low confidence |
| Acute Promyelocytic LeukemiaCI-CAN-00008681Hematologic | Hematologic Malignancy | Acute Myeloid Leukemia with Genetic Abnormalities | 14 | 788 | 16 | 6 | High confidence |
| Acute Promyelocytic Leukemia with a Variant RARA RearrangementCI-CAN-00009228Hematologic | Hematologic Malignancy | Acute Promyelocytic Leukemia, AML with Recurrent Genetic Abnormalities | 0 | 0 | 0 | 9 | Insufficient data |
| Acute Promyelocytic Leukemia with BCOR-RARACI-CAN-00009316Hematologic | Hematologic Malignancy | Acute Promyelocytic Leukemia with a Variant RARA Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Promyelocytic Leukemia with FIP1L1-RARACI-CAN-00009317Hematologic | Hematologic Malignancy | Acute Promyelocytic Leukemia with a Variant RARA Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Promyelocytic Leukemia with STAT3-RARACI-CAN-00009318Hematologic | Hematologic Malignancy | Acute Promyelocytic Leukemia with a Variant RARA Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Promyelocytic Leukemia with STAT5B-RARACI-CAN-00009319Hematologic | Hematologic Malignancy | Acute Promyelocytic Leukemia with a Variant RARA Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Promyelocytic Leukemia with t(11;17)(q13;q21); NUMA1-RARACI-CAN-00009321Hematologic | Molecular Subtype | Acute Promyelocytic Leukemia with a Variant RARA Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Promyelocytic Leukemia with t(11;17)(q23;q21); ZBTB16-RARACI-CAN-00009322Hematologic | Molecular Subtype | Acute Promyelocytic Leukemia with a Variant RARA Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Promyelocytic Leukemia with t(1;17)(q42.3;q21.2); IRF2BP2-RARACI-CAN-00009320Hematologic | Molecular Subtype | Acute Promyelocytic Leukemia with a Variant RARA Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARACI-CAN-00009229Hematologic | Molecular Subtype | Acute Promyelocytic Leukemia | 6 | 3 | 5 | 2 | Medium confidence |
| Acute Promyelocytic Leukemia with t(5;17)(q35;q21); NPM1-RARACI-CAN-00009323Hematologic | Molecular Subtype | Acute Promyelocytic Leukemia with a Variant RARA Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Promyelocytic Leukemia with TBL1XR1-RARACI-CAN-00009324Hematologic | Hematologic Malignancy | Acute Promyelocytic Leukemia with a Variant RARA Rearrangement | 0 | 0 | 0 | 0 | Insufficient data |
| Acute Undifferentiated LeukemiaCI-CAN-00004308Hematologic | Hematologic Malignancy | Acute Leukemia of Ambiguous Lineage | 11 | 284 | 0 | 1 | Low confidence |
| Adamantinoid TrichoblastomaCI-CAN-00007142Non-malignant / precursor | Subtype | Trichoblastoma | 0 | 0 | 0 | 0 | Insufficient data |
| AdamantinomaCI-CAN-00000056 | Cancer | Epithelial Neoplasm, Malignant Bone Neoplasm | 0 | 43 | 0 | 1 | Low confidence |
| Adamantinoma-Like Ewing SarcomaCI-CAN-00001680 | Subtype | Extraskeletal Ewing Sarcoma, High Grade Sarcoma | 0 | 150 | 0 | 2 | Low confidence |
| Adamantinomatous CraniopharyngiomaCI-CAN-00000401Non-malignant / precursor | Subtype | Craniopharyngioma | 5 | 0 | 0 | 2 | Low confidence |
| AdenocarcinofibromaCI-CAN-00000402 | Subtype | Malignant Mixed Neoplasm, Malignant Ovarian Neoplasm, Mixed Mesodermal (Mullerian) Tumor | 2 | 0 | 0 | 3 | Low confidence |
| AdenocarcinomaCI-CAN-00000403 | Histology | Carcinoma, Carcinoma of Unknown Primary, Glandular Cell Neoplasm | 2,751 | 93,894 | 423 | 53 | High confidence |
| Adenocarcinoma in Adenomatous PolypCI-CAN-00001681 | Subtype | Carcinoma in a Polyp, Digestive System Adenocarcinoma | 0 | 1 | 0 | 5 | Low confidence |
| Adenocarcinoma in Adenomatous Polyposis ColiCI-CAN-00007143 | Subtype | Adenocarcinoma in Multiple Adenomatous Polyps | 0 | 0 | 0 | 0 | Insufficient data |
"—" means no counter has been computed for this entity yet (counters appear after the first connector of that domain runs). Data confidence summarizes how many domains hold data; it is not a clinical judgement.