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Explorer
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.
1,831 entities
| Cancer | Type | Parent(s) | Active trials (count) | Publications 5y (count) | Evidence items (count) | Children | Completeness | Data confidence |
|---|---|---|---|---|---|---|---|---|
| Chondrosarcoma, Grade 3CI-CAN-00002353 | Subtype | Chondrosarcoma, High Grade Sarcoma | 2 | 57 | 0 | 2 | Low confidence | |
| Chordoid MeningiomaCI-CAN-00004935Non-malignant / precursor | Subtype | Grade 2 Meningioma, Meningeal Neoplasm | 0 | 0 | 0 | 0 |
| Insufficient data |
| Choroid HemangiomaCI-CAN-00004937Non-malignant / precursor | Subtype | Benign Choroid Neoplasm, Hemangioma | 0 | 0 | 0 | 0 | Insufficient data |
| Choroid Plexus MeningiomaCI-CAN-00004941Non-malignant / precursor | Subtype | Intracranial Meningioma | 0 | 0 | 0 | 0 | Insufficient data |
| CIC-DUX4L SarcomaCI-CAN-00007483 | Subtype | CIC-Rearranged Sarcoma | 0 | 0 | 0 | 0 | Insufficient data |
| CIC-DUX4 SarcomaCI-CAN-00007482 | Subtype | CIC-Rearranged Sarcoma | 0 | 37 | 0 | 0 | Low confidence |
| CIC-Rearranged SarcomaCI-CAN-00004958 | Molecular Subtype | EWSR1-Negative Small Round Cell Tumor | 2 | 97 | 4 | 4 | Medium confidence |
| Ciliary Body LeiomyomaCI-CAN-00004961Non-malignant / precursor | Subtype | Benign Ciliary Body Neoplasm, Leiomyoma | 0 | 0 | 0 | 0 | Insufficient data |
| Classical Low Grade Fibromyxoid SarcomaCI-CAN-00004968 | Subtype | Low Grade Fibromyxoid Sarcoma | 0 | 0 | 0 | 0 | Insufficient data |
| Classic Atypical FibroxanthomaCI-CAN-00002374Non-malignant / precursor | Subtype | Atypical Fibroxanthoma | 0 | 0 | 0 | 0 | Insufficient data |
| Classic Dermatofibrosarcoma ProtuberansCI-CAN-00004964Non-malignant / precursor | Subtype | Dermatofibrosarcoma Protuberans | 0 | 0 | 0 | 0 | Insufficient data |
| Classic Inclusion Body FibromatosisCI-CAN-00004966Non-malignant / precursor | Subtype | Inclusion Body Fibromatosis | 0 | 0 | 0 | 0 | Insufficient data |
| Classic Kaposi SarcomaCI-CAN-00007487 | Subtype | Skin Kaposi Sarcoma | 0 | 53 | 0 | 0 | Low confidence |
| Classic RhabdomyomaCI-CAN-00008807Non-malignant / precursor | Subtype | Fetal Rhabdomyoma | 0 | 0 | 0 | 0 | Insufficient data |
| Clear Cell Atypical FibroxanthomaCI-CAN-00002380Non-malignant / precursor | Subtype | Atypical Fibroxanthoma | 0 | 0 | 0 | 0 | Insufficient data |
| Clear Cell ChondrosarcomaCI-CAN-00002381 | Subtype | Bone Sarcoma, Chondrosarcoma | 1 | 3 | 0 | 0 | Low confidence |
| Clear Cell MeningiomaCI-CAN-00004973Non-malignant / precursor | Subtype | Grade 2 Meningioma, Meningeal Neoplasm | 0 | 0 | 0 | 2 | Insufficient data |
| Clear Cell Myomelanocytic Tumor of the Falciform Ligament/Ligamentum TeresCI-CAN-00004974Non-malignant / precursor | Subtype | PEComa | 0 | 0 | 0 | 0 | Insufficient data |
| Clear Cell Sarcoma of Soft TissueCI-CAN-00002383 | Subtype | Malignant Soft Tissue Neoplasm of Uncertain Differentiation, Soft Tissue Sarcoma | 11 | 125 | 3 | 3 | Medium confidence |
| Clear Cell Sarcoma of the KidneyCI-CAN-00004977Pediatric | Subtype | Childhood Malignant Kidney Neoplasm, Childhood Soft Tissue Sarcoma, Kidney Sarcoma | 0 | 106 | 10 | 0 | Medium confidence |
| Clivus Chondroid ChordomaCI-CAN-00004981 | Subtype | Chondroid Chordoma, Clivus Chordoma | 0 | 0 | 0 | 0 | Insufficient data |
| Clivus ChordomaCI-CAN-00007494 | Subtype | Skull Base Chordoma | 0 | 122 | 0 | 1 | Low confidence |
| Clivus MeningiomaCI-CAN-00007495Non-malignant / precursor | Subtype | Posterior Fossa Meningioma, Skull Base Meningioma | 0 | 0 | 0 | 2 | Insufficient data |
| Coccygeal ChordomaCI-CAN-00007496 | Subtype | Malignant Coccygeal Neoplasm, Spinal Chordoma | 0 | 1 | 0 | 0 | Low confidence |
| Coccygeal NeoplasmCI-CAN-00004982Non-malignant / precursor | Subtype | Spinal Neoplasm | 0 | 0 | 0 | 1 | Insufficient data |
| Colon Cavernous HemangiomaCI-CAN-00002391Non-malignant / precursor | Subtype | Benign Colon Neoplasm, Cavernous Hemangioma, Digestive System Hemangioma | 0 | 0 | 0 | 0 | Insufficient data |
| Colon GanglioneuromaCI-CAN-00008813Non-malignant / precursor | Subtype | Benign Colon Neoplasm, Colorectal Ganglioneuroma | 0 | 0 | 0 | 0 | Insufficient data |
| Colon Gastrointestinal Stromal TumorCI-CAN-00004986Non-malignant / precursor | Subtype | Colon Neoplasm, Colorectal Gastrointestinal Stromal Tumor | 0 | 0 | 0 | 0 | Insufficient data |
| Colon Inflammatory Myofibroblastic TumorCI-CAN-00002392Non-malignant / precursor | Subtype | Colon Neoplasm, Digestive System Inflammatory Myofibroblastic Tumor | 0 | 0 | 0 | 0 | Insufficient data |
| Colon Kaposi SarcomaCI-CAN-00007505 | Subtype | Colon Sarcoma, Colorectal Kaposi Sarcoma | 0 | 3 | 0 | 0 | Low confidence |
| Colon LeiomyomaCI-CAN-00007508Non-malignant / precursor | Subtype | Benign Colon Neoplasm, Colorectal Leiomyoma | 0 | 0 | 0 | 0 | Insufficient data |
| Colon LeiomyosarcomaCI-CAN-00007509 | Subtype | Colon Sarcoma, Colorectal Leiomyosarcoma | 0 | 20 | 0 | 0 | Low confidence |
| Colon LipomaCI-CAN-00007510Non-malignant / precursor | Subtype | Benign Colon Neoplasm, Colorectal Lipoma | 0 | 0 | 0 | 1 | Insufficient data |
| Colon LiposarcomaCI-CAN-00002393 | Subtype | Colon Sarcoma, Liposarcoma | 0 | 1 | 0 | 0 | Low confidence |
| Colon LymphangiomaCI-CAN-00008815Non-malignant / precursor | Subtype | Benign Colon Neoplasm, Intra-Abdominal Lymphangioma | 0 | 0 | 0 | 0 | Insufficient data |
| Colon PEComaCI-CAN-00004994Non-malignant / precursor | Subtype | Colon Neoplasm, Intestinal PEComa | 0 | 0 | 0 | 0 | Insufficient data |
| Colon SarcomaCI-CAN-00007516 | Subtype | Colorectal Sarcoma, Malignant Colon Neoplasm | 0 | 11 | 0 | 3 | Low confidence |
| Colorectal AngiosarcomaCI-CAN-00007521 | Subtype | Colorectal Sarcoma, Visceral Angiosarcoma | 0 | 2 | 0 | 0 | Low confidence |
| Colorectal GanglioneuromaCI-CAN-00007530Non-malignant / precursor | Subtype | Benign Colorectal Neoplasm, Intestinal Ganglioneuroma | 0 | 0 | 0 | 1 | Insufficient data |
| Colorectal Gastrointestinal Stromal TumorCI-CAN-00002397Non-malignant / precursor | Subtype | Colorectal Neoplasm, Gastrointestinal Stromal Tumor of the Gastrointestinal Tract | 1 | 0 | 0 | 3 | Low confidence |
| Colorectal Kaposi SarcomaCI-CAN-00005015 | Subtype | Colorectal Sarcoma, Digestive System Kaposi Sarcoma | 0 | 0 | 0 | 2 | Insufficient data |
| Colorectal LeiomyomaCI-CAN-00005018Non-malignant / precursor | Subtype | Benign Colorectal Neoplasm, Benign Intestinal Soft Tissue Neoplasm, Digestive System Leiomyoma | 0 | 0 | 0 | 2 | Insufficient data |
| Colorectal LeiomyosarcomaCI-CAN-00005019 | Subtype | Colorectal Sarcoma, Digestive System Leiomyosarcoma | 0 | 4 | 0 | 2 | Low confidence |
| Colorectal LipomaCI-CAN-00005020Non-malignant / precursor | Subtype | Benign Colorectal Neoplasm, Benign Intestinal Soft Tissue Neoplasm, Digestive System Lipoma | 0 | 0 | 0 | 2 | Insufficient data |
| Colorectal PerineuriomaCI-CAN-00005027Non-malignant / precursor | Subtype | Benign Colorectal Neoplasm, Benign Intestinal Soft Tissue Neoplasm, Gastrointestinal Tract Perineurioma | 0 | 0 | 0 | 0 | Insufficient data |
| Colorectal SarcomaCI-CAN-00005028 | Subtype | Intestinal Sarcoma, Malignant Colorectal Neoplasm | 0 | 3 | 0 | 6 | Low confidence |
| Colorectal SchwannomaCI-CAN-00005029Non-malignant / precursor | Subtype | Benign Colorectal Neoplasm, Benign Intestinal Soft Tissue Neoplasm, Digestive System Schwannoma | 0 | 0 | 0 | 0 | Insufficient data |
| Composite HemangioendotheliomaCI-CAN-00005037Non-malignant / precursor | Subtype | Hemangioendothelioma, Intermediate (Rarely Metastasizing) Blood Vessel Neoplasm | 0 | 0 | 0 | 2 | Insufficient data |
| Congenital HemangiomaCI-CAN-00007551Non-malignant / precursor | Subtype | Hemangioma | 0 | 0 | 0 | 4 | Insufficient data |
| Congenital/Infantile Spindle Cell Rhabdomyosarcoma with VGLL2/NCOA2/CITED2 RearrangementsCI-CAN-00008827 | Subtype | Spindle Cell Rhabdomyosarcoma | 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.