Informaţii despre

Nume Colorectal Cancer
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare; Bolile canceroase
Clasificari ICD10 Malignant neoplasm: Colon, unspecified
Clasificare anatomică Malacards Boli gastrointestinale
Boli din aceeaşi familie Colorectal Cancer 1; Colorectal Cancer 10; Colorectal Cancer 11; Colorectal Cancer 12; Colorectal Cancer 2; Colorectal Cancer 3; Colorectal Cancer 5; Colorectal Cancer 6; Colorectal Cancer 7; Colorectal Cancer 8; Colorectal Cancer 9; Familial Colorectal Cancer; Familial Colorectal Cancer Type X

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Boli A-Z Aarskog-Scott Syndrome Acetaminophen Metabolism Acinar Cell Carcinoma Acneiform Dermatitis Acquired Hemophilia a Acquired Thrombocytopenia Acral Lentiginous Melanoma Acrocallosal Syndrome Acrodermatitis Enteropathica, Zinc-Deficiency Type Acromegaly Actinic Cheilitis Actinic Keratosis Acute Lymphoblastic Leukemia, Childhood Acute Myocardial Infarction Acute Pancreatitis Adenocarcinoma Adenoma Adenomyoma Adenomyosis Adenosquamous Carcinoma Adenosquamous Colon Carcinoma Adenosquamous Pancreas Carcinoma Adie Pupil Adrenocortical Carcinoma, Hereditary Adult Hepatocellular Carcinoma Aging Alexithymia Allergic Contact Dermatitis Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amenorrhea Ampulla of Vater Adenocarcinoma Ampulla of Vater Neoplasm Amyloidosis Beta2m Anal Canal Carcinoma Anal Squamous Cell Carcinoma Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome Androgen Insensitivity Syndrome, Mild Aneurysm Angel-Shaped Phalangoepiphyseal Dysplasia Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Antipyrine Metabolism Aortic Aneurysm Aortic Valve Disease 2 Apert Syndrome Aplastic Anemia Apocrine Adenoma Appendix Adenocarcinoma Appendix Cancer Appendix Carcinoid Tumor Arterial Tortuosity Syndrome Arthrochalasia Ehlers-Danlos Syndrome Aspergillosis Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Ataxia-Telangiectasia Athabaskan Brainstem Dysgenesis Syndrome Atrophic Gastritis Attenuated Familial Adenomatous Polyposis Autoimmune Myocarditis Autoinflammation, Lipodystrophy, and Dermatosis Syndrome Axenfeld-Rieger Syndrome Barrett's Adenocarcinoma Barrett Esophagus B-Cell Lymphomas Beukes Hip Dysplasia Bilateral Breast Cancer Bile Duct Adenocarcinoma Bile Duct Carcinoma Bile Duct Cystadenocarcinoma Bile Duct Mucoepidermoid Carcinoma Biliary Papillomatosis Biliary Tract Neoplasm Bladder Adenocarcinoma Bladder Cancer Bladder Disease Bladder Papillary Transitional Cell Neoplasm Bladder Transitional Cell Papilloma Bladder Urothelial Carcinoma Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bloom Syndrome Bobble-Head Doll Syndrome Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Bone Squamous Cell Carcinoma Bornholm Eye Disease Brachydactyly Breast Adenocarcinoma Breast Cancer Breast Carcinoma in Situ Breast Ductal Carcinoma Breast Giant Fibroadenoma Broken Heart Syndrome Bronchogenic Cyst Buruli Ulcer Campylobacteriosis Capillary Leak Syndrome Carbuncle Cataract 5, Multiple Types Cayler Cardiofacial Syndrome Cecal Benign Neoplasm Cecum Adenocarcinoma Cell Type Cancer Central Nervous System Tuberculosis Ceroid Lipofuscinosis, Neuronal, 10 Cervical Adenocarcinoma Cervical Cancer Cervical Intraepithelial Neoplasia Cervical Squamous Cell Carcinoma Cervicitis Chagas Disease Chlamydia Cholangiocarcinoma Cholangitis Cholecystitis Cholelithiasis Cholera Chops Syndrome Choroiditis Chronic Enteropathy Associated with Slco2a1 Gene Cicatricial Ectropion Clear Cell Adenocarcinoma Clear Cell Renal Cell Carcinoma Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly Colitis Colon Adenocarcinoma Colon Adenoma Colonic Benign Neoplasm Colorectal Adenocarcinoma Colorectal Adenoma Colorectal Cancer 1 Colorectal Cancer 10 Colorectal Cancer 11 Colorectal Cancer 2 Colorectal Cancer 3 Colorectal Cancer 5 Colorectal Cancer 6 Colorectal Cancer 7 Colorectal Cancer 8 Colorectal Cancer 9 Conjunctivochalasis Conotruncal Heart Malformations Constipation Corneal Dystrophy, Avellino Type Craniodiaphyseal Dysplasia Crohn's Colitis Crouzon Syndrome with Acanthosis Nigricans Cryptosporidiosis Cystadenocarcinoma Cystitis Cytochrome P450 2d6 Variant Cytomegalovirus Infection Deafness, Autosomal Dominant 5 Denys-Drash Syndrome Diabetes Mellitus Diarrhea Dihydropyrimidine Dehydrogenase Deficiency Disseminated Intravascular Coagulation Diverticulitis Donohue Syndrome Dry Eye Syndrome Ductal Carcinoma in Situ Duodenitis Duodenum Cancer Dyschromatosis Symmetrica Hereditaria Eales Disease Ectropion Elastosis Perforans Serpiginosa Embryonal Carcinoma Endocarditis Endocervical Adenocarcinoma Endocervicitis Endometrial Adenocarcinoma Endometrial Cancer Endometriosis Endotheliitis Eosinophilic Gastroenteritis Epidermolysis Bullosa Pruriginosa Epithelial Recurrent Erosion Dystrophy Epstein-Barr Virus-Associated Gastric Carcinoma Esophageal Cancer Estrogen Resistance Factor Vii Deficiency Fallopian Tube Carcinoma Familial Adenomatous Polyposis Familial Adenomatous Polyposis 1 Familial Colorectal Cancer Familial Colorectal Cancer Type X Fanconi Anemia, Complementation Group D2 Fanconi Anemia, Complementation Group E Fatty Liver Disease Fecal Incontinence Female Reproductive Organ Cancer Fetal Alcohol Syndrome Fibromatosis, Gingival, 1 Fibrosarcoma Fibrous Histiocytoma Filariasis Follicular Lymphoma Fournier Gangrene Friedreich Ataxia 1 Fundus Albipunctatus Galactose Epimerase Deficiency Gallbladder Cancer Ganglioneuroma Gastric Adenocarcinoma Gastric Cancer Gastric Diffuse Adenocarcinoma Gastric Lymphoma Gastric Tubular Adenocarcinoma Gastric Ulcer Gastritis Gastroesophageal Junction Adenocarcinoma Gastrointestinal Carcinoma Gastrointestinal Defects and Immunodeficiency Syndrome Gastrointestinal Stromal Tumor Gastrointestinal System Benign Neoplasm Gastrointestinal System Cancer Genitopatellar Syndrome Gerstmann Syndrome Gilles De La Tourette Syndrome Gingival Recession Gingivitis Gitelman Syndrome Glaucoma-Related Pigment Dispersion Syndrome Glioblastoma Glioblastoma Multiforme Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Glucose Intolerance Glucosephosphate Dehydrogenase Deficiency Glycogen-Rich Clear Cell Breast Carcinoma Goblet Cell Carcinoid Grade Iii Astrocytoma Griscelli Syndrome Growth Control, Y-Chromosome Influenced Guillain-Barre Syndrome Headache Associated with Sexual Activity Helicobacter Pylori Infection Hemangioma Hemangioma-Thrombocytopenia Syndrome Hemophagocytic Lymphohistiocytosis, Familial, 2 Hemorrhoid Hepatic Adenomas, Familial Hepatic Tuberculosis Hepatitis Hepatoblastoma Hepatocellular Carcinoma Hereditary Hemorrhagic Telangiectasia Hereditary Wilms' Tumor Hidradenocarcinoma Histiocytoma Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperaldosteronism, Familial, Type I Hyperandrogenism Hypercholesterolemia, Autosomal Dominant, 3 Hyperphosphatemia Hyperplastic Polyposis Syndrome Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertrophic Scars Hypocalcemia, Autosomal Dominant 1 Hypogonadotropic Hypogonadism 1 with or Without Anosmia Hypoparathyroidism, Familial Isolated Hypophosphatasia, Adult Hypophosphatasia, Infantile Hypoxia Ichthyosis Vulgaris Ileocolitis Immune Suppression Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 Infective Dermatitis Associated with Htlv-1 Infective Endocarditis Inflammatory Bowel Disease Insulin-Like Growth Factor I Internal Hemorrhoid Interstitial Lung Disease Intestinal Benign Neoplasm Intestinal Perforation Intestinal Schistosomiasis Intestinal Tuberculosis Intrahepatic Cholangiocarcinoma Invasive Aspergillosis Irinotecan Toxicity Irritable Bowel Syndrome Ischemia Janus Kinase-3 Deficiency Jejunal Adenocarcinoma Juvenile Nasopharyngeal Angiofibroma Juvenile Polyposis Syndrome Juxtacortical Osteosarcoma Kabuki Syndrome 1 Kashin-Beck Disease Keloids Keratocystic Odontogenic Tumor Kidney Cancer Lactose Intolerance Larynx Cancer Laurence-Moon Syndrome Learning Disability Leiomyosarcoma Leopard Syndrome Lepromatous Leprosy Leukemia Leukostasis Li-Fraumeni Syndrome Li-Fraumeni Syndrome 2 Lip Cancer Liposarcoma Lissencephaly 1 Liver Cirrhosis Liver Disease Lobular Neoplasia Localized Scleroderma Logopenic Progressive Aphasia Long Qt Syndrome 1 Lung Cancer Lung Cancer Susceptibility 3 Lung Disease Lung Giant Cell Carcinoma Lupus Erythematosus Lymphadenitis Lymphangioma Lymphedema, Hereditary, Ia Lymph Node Cancer Lymph Node Disease Lymphoepithelioma-Like Carcinoma Lymphoma Lymphopenia Lynch Syndrome Lynch Syndrome I Mal De Meleda Malignant Glioma Malignant Ovarian Cyst Malignant Ovarian Surface Epithelial-Stromal Neoplasm Mammary Paget's Disease Mantle Cell Lymphoma Marantic Endocarditis Marshall-Smith Syndrome Maturity-Onset Diabetes of the Young Mckusick-Kaufman Syndrome Melanoma Melanoma Metastasis Menkes Disease Microcystic Meningioma Microinvasive Gastric Cancer Microscopic Colitis Microvascular Complications of Diabetes 1 Migraine with or Without Aura 1 Mismatch Repair Cancer Syndrome Mitochondrial Neurogastrointestinal Encephalopathy Disease Mohr-Tranebjaerg Syndrome Mucinous Adenocarcinoma Mucinous Bronchioloalveolar Adenocarcinoma Mucinous Tubular and Spindle Renal Cell Carcinoma Mucoepidermoid Carcinoma Mucositis Muir-Torre Syndrome Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 Multiple Mitochondrial Dysfunctions Syndrome 5 Mungan Syndrome Mutagen Sensitivity Mutyh-Associated Polyposis Myasthenia Gravis Mycobacterium Kansasii Myeloid Leukemia Myeloma, Multiple Myocardial Infarction Nasal Cavity Adenocarcinoma Netherton Syndrome Neuraminidase Deficiency Neuroblastoma Neurodegeneration with Brain Iron Accumulation 2a Neuroendocrine Tumor Neuronitis Neuropathy Neutropenia Neutrophil Actin Dysfunction Neutrophilic Dermatosis, Acute Febrile Nevus, Epidermal Nodular Goiter Non-Involuting Congenital Hemangioma Noonan Syndrome 1 Obstructive Jaundice Occipital Horn Syndrome Ocular Cancer Oral Cancer Oral Cavity Cancer Oral Leukoplakia Oral Squamous Cell Carcinoma Oral Submucous Fibrosis Orotic Aciduria Ovarian Cancer Ovarian Cancer 1 Ovarian Mucinous Adenocarcinoma Ovary Epithelial Cancer Overhydrated Hereditary Stomatocytosis Paine Syndrome Palmoplantar Keratoderma, Punctate Type Iii Pancreas Adenocarcinoma Pancreatic Cancer Pancreatic Ductal Adenocarcinoma Pancreatic Ductal Carcinoma Pancreatic Intraductal Papillary-Mucinous Neoplasm Pancreatic Mucinous Cystadenoma Pancreatitis Papillary Adenocarcinoma Papillary Carcinoma Papilloma Paracoccidioidomycosis Parkinson Disease 2, Autosomal Recessive Juvenile Parkinsonism with Spasticity, X-Linked Parotid Gland Cancer Pelvic Inflammatory Disease Pericholangitis Periodontal Disease Periodontitis Periodontitis, Aggressive, 1 Peritonitis Pernicious Anemia Persistent Idiopathic Facial Pain Peutz-Jeghers Syndrome Peyronie's Disease Pheochromocytoma Phosphoserine Phosphatase Deficiency Pituitary Adenoma 1, Multiple Types Pituitary Apoplexy Pituitary Tumors Plasma Cell Leukemia Pleomorphic Adenoma Pleomorphic Carcinoma Pleomorphic Rhabdomyosarcoma Pneumoconiosis Polyposis Syndrome, Hereditary Mixed, 1 Porokeratosis Portal Hypertension Primary Effusion Lymphoma Primary Peritoneal Carcinoma Proctitis Proliferating Trichilemmal Cyst Prostate Cancer Prostatitis Protein C Deficiency Pseudo-Meigs Syndrome Pseudomyxoma Peritonei Pulmonary Edema Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Sclerosing Hemangioma Pulmonic Stenosis Rectal Neoplasm Relapsing-Remitting Multiple Sclerosis Renal Clear Cell Carcinoma Renal Glucosuria Reproductive Organ Cancer Retinal Cancer Retinal Ischemia Retinitis Retinoblastoma Retinoschisis 1, X-Linked, Juvenile Rett Syndrome Reye Syndrome Rhabdomyosarcoma Rheumatic Disease Richards-Rundle Syndrome Ring Chromosome 1 Ring Chromosome 2 Roberts Syndrome Robinow Syndrome, Autosomal Recessive Salivary Gland Adenoid Cystic Carcinoma Salivary Gland Adenoma, Pleomorphic Salivary Gland Cancer Sarcoidosis 2 Sarcoma Sarcosinemia Schimmelpenning-Feuerstein-Mims Syndrome Schistosomiasis Schizophrenia Sclerosing Cholangitis Sclerosing Cholangitis, Neonatal Sclerosing Hemangioma Sebaceous Adenoma Secretory Meningioma Sensory System Cancer Serous Cystadenocarcinoma Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Short-Rib Thoracic Dysplasia 9 with or Without Polydactyly Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Short Stature, Developmental Delay, and Congenital Heart Defects Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Signet Ring Cell Adenocarcinoma Situs Inversus Skin Melanoma Skin Tag Small Intestinal Adenocarcinoma Small Intestine Cancer Soft Tissue Sarcoma Somatostatinoma Spasticity Spastic Paraplegia 20, Autosomal Recessive Spinal Chordoma Spiradenoma Spitz Nevus Splenic Tuberculosis Splenomegaly Spondyloocular Syndrome Sporadic Breast Cancer Squamous Cell Carcinoma Squamous Cell Carcinoma, Head and Neck Squamous Cell Carcinoma of the Hypopharynx Squamous Cell Carcinoma of the Larynx Stomatitis Suppressor of Tumorigenicity 3 Sveinsson Chorioretinal Atrophy Synchronous Bilateral Breast Carcinoma Systemic Capillary Leak Syndrome Systemic Lupus Erythematosus Takenouchi-Kosaki Syndrome T-Cell Leukemia Tetanus Tetraploidy Thrombocytopenia Thrombocytosis Thyroid Cancer, Nonmedullary, 2 Thyroiditis Timothy Syndrome Tongue Cancer Tongue Squamous Cell Carcinoma Tonsillitis Tooth Agenesis Toxic Shock Syndrome Toxoplasmoză Transcobalamin Ii Deficiency Transitional Cell Carcinoma Trichomegaly Tropical Spastic Paraparesis Trypanosomiasis Tuberous Sclerosis 1 Tuberous Sclerosis 2 Tubular Adenocarcinoma Tubulin, Beta Tumor of Exocrine Pancreas Tumor Suppressor Gene on Chromosome 11 Ulcerative Colitis Urinary Tract Papillary Transitional Cell Benign Neoplasm Uterine Carcinosarcoma Vaccinia Van Der Woude Syndrome 1 Vascular Disease Villous Adenoma Virus-Associated Trichodysplasia Spinulosa Visceral Leishmaniasis Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Werner Syndrome Wilms Tumor 6 Wilson Disease Wilson-Turner X-Linked Mental Retardation Syndrome Witkop Syndrome Zollinger-Ellison Syndrome