Informaţii despre

Nume Prostate Cancer
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare; Bolile canceroase
Clasificari ICD10 Malignant neoplasm of prostate
Clasificare anatomică Malacards Boli ale sistemului reproducator
Boli din aceeaşi familie Prostate Cancer, Hereditary, 1; Prostate Cancer, Hereditary, 10; Prostate Cancer, Hereditary, 11; Prostate Cancer, Hereditary, 12; Prostate Cancer, Hereditary, 13; Prostate Cancer, Hereditary, 14; Prostate Cancer, Hereditary, 15; Prostate Cancer, Hereditary, 2; Prostate Cancer, Hereditary, 3; Prostate Cancer, Hereditary, 4; Prostate Cancer, Hereditary, 5; Prostate Cancer, Hereditary, 6; Prostate Cancer, Hereditary, 7; Prostate Cancer, Hereditary, 8; Prostate Cancer, Hereditary, 9; Prostate Carcinoma in Situ

Vezi şi

Boli A-Z Aarskog-Scott Syndrome Ablepharon-Macrostomia Syndrome Acneiform Dermatitis Acquired Color Blindness Acquired Hemophilia Acquired Hemophilia a Acrocallosal Syndrome Acrodermatitis Enteropathica, Zinc-Deficiency Type Acute Lymphocytic Leukemia Adamantinoma of Long Bones Adenocarcinoma Adenoiditis Adenoma Adenomyosis Adenosquamous Carcinoma Adie Pupil Adult Hepatocellular Carcinoma Aging Aicar Transformylase/imp Cyclohydrolase Deficiency Alopecia Alopecia, Androgenetic, 1 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-2-Macroglobulin Deficiency Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amaurosis Fugax Ameloblastoma Amyloidosis, Primary Localized Cutaneous, 1 Anauxetic Dysplasia 1 Androgenic Alopecia Androgen Insensitivity, Partial Androgen Insensitivity Syndrome Androgen Insensitivity Syndrome, Mild Aneurysm of Sinus of Valsalva Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Antigen Defined by Monoclonal Antibody Aj9 Aortic Valve Disease 2 Apert Syndrome Aplastic Anemia Aromatase Deficiency Arthrochalasia Ehlers-Danlos Syndrome Astrocytoma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Atherosclerosis Susceptibility Aural Atresia, Congenital Axenfeld-Rieger Syndrome Back Pain Bacteriuria Basal Cell Carcinoma Bilateral Breast Cancer Bladder Cancer Bladder Transitional Cell Papilloma Blau Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Group--Kell System Blood Group--Wright Antigen 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 Cancer Bone Fracture Bone Lymphoma Bone Marrow Necrosis Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bornholm Eye Disease Brain Edema Brain Ependymoma Brca1 Hereditary Breast and Ovarian Cancer Syndrome Breast Adenocarcinoma Breast Cancer Breast Carcinoma in Situ Breast Cyst Breast Disease Breast Ductal Carcinoma Breast Metaplastic Carcinoma Breast-Ovarian Cancer, Familial 1 Brody Myopathy Broken Heart Syndrome Brunner Syndrome Carbuncle Cardiac Conduction Defect Cell Type Cancer Cervical Adenocarcinoma Cervical Cancer Cervical Squamous Cell Carcinoma Cervicitis Choanal Atresia, Posterior Cholelithiasis Cholestasis-Lymphedema Syndrome Cholesteatoma of Middle Ear Chromosome 8p Deletion Chronic Diarrhea Due to Glucoamylase Deficiency Chronic Enteropathy Associated with Slco2a1 Gene Chronic Fatigue Syndrome Cleft Larynx, Posterior Cohen-Gibson Syndrome Colchicine Resistance Coloboma, Ocular, Autosomal Dominant Color Blindness Colorblindness, Partial, Protan Series Colorectal Adenoma Colorectal Cancer Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complete Androgen Insensitivity Syndrome Congenital Disorder of Glycosylation, Type Iic Congestive Heart Failure Conjunctivitis Cortical Blindness Coumarin Resistance Cranial Nerve Palsy Crouzon Syndrome with Acanthosis Nigricans Cutaneous Mastocytosis Cystic Fibrosis Cystitis Cystitis Cystica Cytochrome P450 2d6 Variant Delayed Sleep Phase Disorder Denys-Drash Syndrome Dermatomyositis Diabetes Insipidus Diabetes Mellitus Diabetes Mellitus, Transient Neonatal, 1 Diffuse Gastric Cancer Disseminated Intravascular Coagulation Donohue Syndrome Doyne Honeycomb Retinal Dystrophy Drug Dependence Duane Retraction Syndrome 1 Ductal Carcinoma in Situ Dyschromatosis Symmetrica Hereditaria Ectopic Cushing Syndrome Endometrial Adenocarcinoma Endometrial Adenosquamous Carcinoma Endometrial Cancer Endometrial Clear Cell Adenocarcinoma Endometriosis Endotheliitis Eosinophilia, Familial Epidermolysis Bullosa Pruriginosa Epiphyseal Dysplasia, Multiple, 1 Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus Epithelial Recurrent Erosion Dystrophy Esophageal Cancer Estrogen-Receptor Positive Breast Cancer Evans' Syndrome Ewing Sarcoma Exanthem Exophthalmos Extracranial Arteriovenous Malformation Facial Paralysis Fallopian Tube Carcinoma Familial Adenomatous Polyposis Fanconi Anemia, Complementation Group E Fasciitis Fecal Incontinence Female Reproductive Organ Cancer Fibromatosis, Gingival, 1 Fibrosarcoma Fibrous Dysplasia Floating-Harbor Syndrome Focal Cortical Dysplasia, Type Ii Foot Drop Fournier Gangrene Friedreich Ataxia 1 Functioning Pituitary Adenoma Fundus Albipunctatus Gallbladder Adenocarcinoma Gallbladder Cancer Gastric Adenocarcinoma Gastric Cancer Gastrointestinal System Cancer Glioblastoma Glioblastoma Multiforme Glioma Glomerulonephritis Glucocorticoid Resistance, Generalized Glucose Intolerance Glucose Transporter Type 1 Deficiency Syndrome Gonadoblastoma Gout Grade Iii Astrocytoma Granular Cell Tumor Greig Cephalopolysyndactyly Syndrome Gynecomastia Headache Associated with Sexual Activity Hemimegalencephaly Hemochromatosis, Neonatal Hemolytic-Uremic Syndrome Hemophagocytic Lymphohistiocytosis, Familial, 2 Hemophilia Hemophilia a Hemorrhagic Cystitis Hepatic Adenomas, Familial Hepatitis Hepatitis C Hepatocellular Carcinoma Hereditary Wilms' Tumor Herpes Simplex Hidradenocarcinoma Human Herpesvirus 8 Human T-Cell Leukemia Virus Type 1 Hydrocele Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius Hydronephrosis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperandrogenism Hypercholesterolemia, Autosomal Dominant, 3 Hyperglycemia Hyperprolactinemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrichosis Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypogonadism Hypophosphatemia Hypophosphatemic Bone Disease Hypotrichosis 1 Hypoxia Ichthyosis Prematurity Syndrome Ichthyosis Vulgaris Immunodeficiency 43 Immunoglobulin E Concentration, Serum Impotence Incontinentia Pigmenti Infant Gynecomastia Infertility Insulin-Like Growth Factor I Intracranial Hypertension Isolated Optic Neuritis Juxtacortical Osteosarcoma Keratocystic Odontogenic Tumor Kidney Cancer Lactic Acidosis Lactose Intolerance Large Cell Neuroendocrine Carcinoma Larynx Cancer Laugier-Hunziker Syndrome Leiomyoma Leiomyoma, Uterine Leiomyosarcoma Leukemia Leukemia, Chronic Lymphocytic 2 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Leydig Cell Tumor Li-Fraumeni Syndrome Li-Fraumeni Syndrome 2 Linear Skin Defects with Multiple Congenital Anomalies 1 Lipid Metabolism Disorder Liposarcoma Lobular Neoplasia Logopenic Progressive Aphasia Long Qt Syndrome 1 Luminal Breast Carcinoma Lung Benign Neoplasm Lung Cancer Lung Cancer Susceptibility 3 Lung Giant Cell Carcinoma Lung Squamous Cell Carcinoma Lymph Node Cancer Lymphoblastic Leukemia Lymphocele Lymphoma Lynch Syndrome Macs Syndrome Malakoplakia Male Infertility Male Reproductive Organ Cancer Malignant Glioma Malignant Ovarian Surface Epithelial-Stromal Neoplasm Malignant Spiradenoma Mammographic Density Mantle Cell Lymphoma Mcleod Syndrome Measles Meckel Syndrome, Type 1 Melancholia Melanoma Membranous Nephropathy Meninges Hemangiopericytoma Meningioma, Familial Mevalonic Aciduria Microscopic Polyangiitis Migraine with or Without Aura 1 Miller-Dieker Lissencephaly Syndrome Mixed Cell Type Cancer Mohr-Tranebjaerg Syndrome Muenke Syndrome Multiple Endocrine Neoplasia Multiple Mitochondrial Dysfunctions Syndrome 5 Mungan Syndrome Muscular Atrophy Mutagen Sensitivity Mycetoma Myeloma, Multiple Myocardial Infarction Myopathy, Myosin Storage, Autosomal Recessive Myotonia, Potassium-Aggravated Necrotizing Fasciitis Nephrogenic Adenoma of the Urethra Nephrotic Syndrome Nervous System Cancer Nestor-Guillermo Progeria Syndrome Neuraminidase Deficiency Neurenteric Cyst Neuroblastoma Neurodegeneration with Brain Iron Accumulation 2a Neuroendocrine Tumor Neuronitis Neutropenia Neutrophil Actin Dysfunction Neutrophilic Dermatosis, Acute Febrile Newcastle Disease Nijmegen Breakage Syndrome Nodular Prostate Non-Functioning Pituitary Adenoma Non-Involuting Congenital Hemangioma Occipital Horn Syndrome Ocular Albinism Ocular Cancer Oncogenic Osteomalacia Oral Cancer Oral Cavity Cancer Oral Squamous Cell Carcinoma Oral Submucous Fibrosis Osteogenic Sarcoma Osteomalacia Osteonecrosis Osteonecrosis of the Jaw Osteopoikilosis Osteoporotic Fracture Ovarian Cancer Ovarian Cancer 1 Ovarian Clear Cell Carcinoma Ovary Epithelial Cancer Overhydrated Hereditary Stomatocytosis Pachyonychia Congenita 3 Paget's Disease of Bone Paget Disease of Bone 3 Pallister-Hall Syndrome Pancreatic Cancer Pancreatitis Pancreatitis, Hereditary Panniculitis Papilloma Papillon-Lefevre Syndrome Paracoccidioidomycosis Parametritis Paraneoplastic Pemphigus Paraneoplastic Syndromes Paraplegia Parkinsonism with Spasticity, X-Linked Parotid Gland Cancer Peeling Skin Syndrome 4 Peliosis Hepatis Pemphigus Pemphigus Foliaceus Penis Agenesis Periodontal Disease Periodontal Ehlers-Danlos Syndrome Periodontitis Periosteal Osteogenic Sarcoma Pernicious Anemia Phelan-Mcdermid Syndrome Pitt-Hopkins Syndrome Pituitary Adenoma Pituitary Adenoma 1, Multiple Types Pituitary Apoplexy Pleomorphic Adenoma Polykaryocytosis Inducer Polymicrogyria, Bilateral Perisylvian, X-Linked Polyneuropathy Posterior Cortical Atrophy Potocki-Lupski Syndrome Pouchitis Pre-Malignant Neoplasm Premature Chromatid Separation Trait Priapism Primary Bone Lymphoma Primary Effusion Lymphoma Primary Lateral Sclerosis, Adult, 1 Proctitis Progesterone-Receptor Positive Breast Cancer Prolymphocytic Leukemia Prostate Cancer Aggressiveness Quantitative Trait Locus on Chromosome 19 Prostate Cancer, Hereditary, 1 Prostate Cancer, Hereditary, 10 Prostate Cancer, Hereditary, 14 Prostate Cancer, Hereditary, 15 Prostate Cancer, Hereditary, 2 Prostate Cancer, Hereditary, 3 Prostate Cancer, Hereditary, 4 Prostate Cancer, Hereditary, 5 Prostate Cancer, Hereditary, 6 Prostate Cancer, Hereditary, 7 Prostate Cancer, Hereditary, 8 Prostate Cancer, Hereditary, 9 Prostate Disease Prostatic Adenoma Prostatic Hyperplasia, Benign Prostatic Hypertrophy Prostatitis Prostatocystitis Proteus Syndrome Pulmonary Disease, Chronic Obstructive Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pure Red-Cell Aplasia Purpura Q Fever Quadriplegia Radiation Cystitis Radiation Proctitis Rapp-Hodgkin Syndrome Rectal Neoplasm Rectosigmoid Junction Neoplasm Reproductive Organ Cancer Retinal Cancer Retinal Hemangioblastoma Retinoblastoma Retroperitoneal Fibrosis Rett Syndrome Ring Chromosome 2 Ring Chromosome 7 Roberts Syndrome Salivary Gland Adenoma, Pleomorphic Salivary Gland Cancer Sarcoma Satb2-Associated Syndrome Schnyder Corneal Dystrophy Sclerosteosis 1 Seminal Vesicle Adenocarcinoma Seminoma Sensory System Cancer Serous Cystadenocarcinoma Severe Combined Immunodeficiency Sex Differentiation Disease Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Short Syndrome Silent Pituitary Adenoma Skin Melanoma Small Cell Carcinoma Soft Tissue Sarcoma Spastic Entropion Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinal Chordoma Sporadic Breast Cancer Squamous Cell Carcinoma Squamous Cell Carcinoma, Head and Neck Squamous Cell Carcinoma of the Larynx Stomatitis Subacute Cerebellar Degeneration Submandibular Gland Cancer Suppression of Tumorigenicity 12 Suppressor of Tumorigenicity 3 Supravalvular Aortic Stenosis Surfactant Metabolism Dysfunction, Pulmonary, 2 Surfactant Metabolism Dysfunction, Pulmonary, 3 Surfactant Metabolism Dysfunction, Pulmonary, 4 Sveinsson Chorioretinal Atrophy Sweat Gland Cancer Synchronous Bilateral Breast Carcinoma Syndrome of Inappropriate Antidiuretic Hormone Syphilis Syringocystadenoma Papilliferum Takenouchi-Kosaki Syndrome Tarp Syndrome T-Cell Lymphoma 1a T-Cell Prolymphocytic Leukemia Thoracoabdominal Syndrome Thrombocytopenia Thrombosis Thrombotic Thrombocytopenic Purpura Thyroiditis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Tongue Cancer Tongue Squamous Cell Carcinoma Transcobalamin I Deficiency Transitional Cell Carcinoma Transsexualism Transsexuality Trichohepatoenteric Syndrome 1 Trichorhinophalangeal Syndrome, Type I Tuberous Sclerosis Tumor Suppressor Gene on Chromosome 11 Ureterocele Urethral Diverticulum Urethral Stricture Urethritis Urticaria Uterine Carcinosarcoma Uterine Corpus Serous Adenocarcinoma Vaccinia Wilms Tumor 6 Witkop Syndrome X-Ray Sensitivity