Informaţii despre

Nume Ring Chromosome Y Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli rare
Clasificari ICD10 Male with structurally abnormal sex chromosome
Clasificare anatomică Malacards Boli neuronale
Boli din aceeaşi familie Ring Chromosome 1; Ring Chromosome 10; Ring Chromosome 11; Ring Chromosome 12; Ring Chromosome 13; Ring Chromosome 14 Syndrome; Ring Chromosome 15; Ring Chromosome 16; Ring Chromosome 17; Ring Chromosome 18; Ring Chromosome 19; Ring Chromosome 2; Ring Chromosome 20; Ring Chromosome 21; Ring Chromosome 22; Ring Chromosome 3; Ring Chromosome 4; Ring Chromosome 5; Ring Chromosome 6; Ring Chromosome 7; Ring Chromosome 8; Ring Chromosome 9

Vezi şi

Boli A-Z 2-Methylbutyryl-Coa Dehydrogenase Deficiency 6-Phosphogluconate Dehydrogenase Deficiency Ablepharon-Macrostomia Syndrome Acquired Immunodeficiency Syndrome Acrocallosal Syndrome Acrofacial Dysostosis, Catania Type Acromegaly Acth-Secreting Pituitary Adenoma Acute Cholinergic Dysautonomia Acute Diarrhea Acute Leukemia Acute Leukemia of Ambiguous Lineage Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) Acute Myocardial Infarction Acute Respiratory Distress Syndrome Adenocarcinoma Adenoma Adult T-Cell Leukemia Aging Agoraphobia Alcohol Dependence Allergic Bronchopulmonary Aspergillosis Allergic Bronchopulmonary Aspergillosis, Familial Allergic Contact Dermatitis Allergic Encephalomyelitis Allergic Rhinitis Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alopecia Universalis Congenita 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 Amblyopia Amelogenesis Imperfecta, Type Iv Amyloidosis Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome Aneurysm Aneurysmal Bone Cysts Angina Pectoris Angioid Streaks Angiomyolipoma Angiostrongyliasis Aniridia 1 Anorexia Nervosa 1 Anovulation Anterograde Amnesia Anteroseptal Myocardial Infarction Antisocial Personality Disorder Aortopulmonary Window Aphasia Apraxia Argentine Hemorrhagic Fever Arteries, Anomalies of Arthritis Arthrochalasia Ehlers-Danlos Syndrome Asbestos Intoxication Asbestosis Aspergillosis Asthma Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Attention Deficit-Hyperactivity Disorder Autism Autoimmune Disease Autoimmune Encephalitis Autoimmune Lymphoproliferative Syndrome, Type V Autonomic Neuropathy Avoidant Personality Disorder Azoospermia Babesiosis B-Cell Lymphomas B Cell Prolymphocytic Leukemia Beriberi Bernard-Soulier Syndrome Bipolar Disorder Bladder Cancer Blastomycosis Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Blood Group, Junior System Blood Group--Wright Antigen Body Dysmorphic Disorder 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 Lymphoma Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Borderline Personality Disorder Brain Edema Brain Injury Breast Cancer Breast Disease Breast Reconstruction Bronchiolitis Bronchiolitis Obliterans Burkitt Lymphoma Burns Castleman Disease Cataract Central Nervous System Lymphoma Cerebellar Degeneration Cerebral Palsy Cerebritis Cervical Cancer Cervicitis Charcot-Marie-Tooth Disease Chikungunya Childhood Apraxia of Speech Chlamydia Cholangiocarcinoma Cholestasis-Lymphedema Syndrome Cholesteatoma Chops Syndrome Choriocarcinoma Chronic Enteropathy Associated with Slco2a1 Gene Chronic Fatigue Syndrome Chronic Granulomatous Disease Chronic Myelomonocytic Leukemia Chronic Pain Clear Cell Renal Cell Carcinoma Cleft Larynx, Posterior Clostridium Difficile Colitis Cocaine Dependence Coccidioidomycosis Colitis Colon Adenocarcinoma Colon Adenoma Color Blindness Colorectal Adenocarcinoma Colorectal Cancer Common Variable Immunodeficiency Compartment Syndrome Complement Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complete Androgen Insensitivity Syndrome Complex Regional Pain Syndrome Congenital Anomalies of Kidney and Urinary Tract 2 Congenital Disorder of Glycosylation, Type Iic Congenital Ichthyosiform Erythroderma Congestive Heart Failure Constipation Contact Dermatitis Conversion Disorder Corneal Dystrophy Corneal Dystrophy, Reis-Bucklers Type Corneal Dystrophy, Thiel-Behnke Type Coronary Artery Anomaly Corticobasal Degeneration Corticosteroid-Binding Globulin Deficiency Creutzfeldt-Jakob Disease Cutaneous Leishmaniasis Cystic Fibrosis Cystitis Cytochrome P450 2d6 Variant Danon Disease Deafness-Hypogonadism Syndrome Degenerative Disc Disease Delusional Disorder Dementia Dependent Personality Disorder Depersonalization Disorder Dermatitis Dermatitis Herpetiformis, Familial Dermatofibrosarcoma Protuberans Dextrocardia Diabetes Mellitus Diabetic Autonomic Neuropathy Diabetic Neuropathy Diarrhea Differentiated Thyroid Carcinoma Diffuse Large B-Cell Lymphoma Digeorge Syndrome Dilated Cardiomyopathy Diphtheria Discoid Lupus Erythematosus Disease_ontology Disseminated Intravascular Coagulation Dissociative Disorder Dowling-Degos Disease 1 Down Syndrome Drug Dependence Dysautonomia Dysentery Early-Onset Schizophrenia Eating Disorder Echinococcosis Eclampsia Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome, Classic Type, 1 Encephalitis Encephalopathy Endocarditis Endocrine Gland Cancer Endogenous Depression Endometrial Adenocarcinoma Endometrial Cancer Endometriosis Endotheliitis Enterobiasis Epidemic Typhus Epidermolysis Bullosa Pruriginosa Epididymo-Orchitis Epilepsy Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus Epithelial Recurrent Erosion Dystrophy Erysipelas Essential Thrombocythemia Estrogen Resistance Fanconi Anemia, Complementation Group E Febrile Infection-Related Epilepsy Syndrome Febrile Seizures Feingold Syndrome 1 Female Stress Incontinence Focal Epilepsy Follicular Lymphoma Foxp2-Related Speech and Language Disorders Fragile X-Associated Tremor/ataxia Syndrome Fragile X Syndrome Fragile X Tremor/ataxia Syndrome Friedreich Ataxia 1 Frozen Shoulder Fundus Albipunctatus Gastric Adenocarcinoma Gastric Cancer Gastroenteritis Gastroschisis Germ Cells Tumors Gerstmann Syndrome Gilles De La Tourette Syndrome Gingivitis Gitelman Syndrome Glioblastoma Glioma Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Glomerulonephritis Glucose Transporter Type 1 Deficiency Syndrome Gout Gray Zone Lymphoma Griscelli Syndrome Growth Control, Y-Chromosome Influenced Growth Hormone Deficiency Haim-Munk Syndrome Hajdu-Cheney Syndrome Headache Associated with Sexual Activity Head Injury Helix Syndrome Hemochromatosis, Neonatal Hemolytic Anemia Hemophilia Hemophilia B Hemorrhagic Cystitis Hemorrhagic Fever Hemorrhoid Heparin-Induced Thrombocytopenia Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatitis Hepatitis B Hepatitis C Hepatitis C Virus Hepatocellular Carcinoma Hermaphroditism Heroin Dependence Herpes Simplex Histidinemia Histiocytosis Histoplasmosis Histrionic Personality Disorder Human Coronavirus Sensitivity Human Immunodeficiency Virus Type 1 Human T-Cell Leukemia Virus Type 1 Hydronephrosis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperaldosteronism, Familial, Type I Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant Hypercholesterolemia, Autosomal Dominant, 3 Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Heart Disease Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypochondriasis Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypophosphatemia Hypospadias Hypoxia Immunoglobulin E Concentration, Serum Impotence Indian Tick Typhus Indolent B Cell Lymphoma Infective Endocarditis Inferior Myocardial Infarction Infertility Inflammatory Bowel Disease Influenza Insulin-Like Growth Factor I Insulinoma Intermittent Claudication Intravascular Large B-Cell Lymphoma Ischemia Ischemic Optic Neuropathy Ischemic Retinopathy Isolated Growth Hormone Deficiency Japanese Encephalitis Kagami-Ogata Syndrome Kallmann Syndrome Kaufman Oculocerebrofacial Syndrome Kawasaki Disease Keratoconus Kernicterus Kidney Cancer Klippel-Trenaunay-Weber Syndrome Labyrinthitis Landau-Kleffner Syndrome Langerhans Cell Histiocytosis Langer Mesomelic Dysplasia Laryngitis Laryngotracheitis Larynx Cancer Lateral Myocardial Infarction Lateral Sclerosis Laugier-Hunziker Syndrome Learning Disability Leiomyoma Leiomyosarcoma Leishmaniasis Leri-Weill Dyschondrosteosis Leukemia Lipodystrophy Lissencephaly 1 Liver Cirrhosis Long Qt Syndrome 1 Lung Cancer Lupus Erythematosus Luscan-Lumish Syndrome Lymphedema, Hereditary, Ia Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphoma Lymphoma, Mucosa-Associated Lymphoid Type Lymphoplasmacytic Lymphoma Lymphosarcoma Macroglobulinemia Malaria Male Infertility Malignant Pleural Mesothelioma Malignant Spiradenoma Mantle Cell Lymphoma Maple Syrup Urine Disease Mastoiditis Measles Meckel Syndrome, Type 1 Mediastinitis Meester-Loeys Syndrome Megakaryocytic Leukemia Melancholia Melanoma Membranous Nephropathy Meningitis Metabolic Acidosis Microcephaly Microcephaly, Epilepsy, and Diabetes Syndrome Microscopic Colitis Microtia-Anotia Migraine with or Without Aura 1 Miller-Dieker Lissencephaly Syndrome Moebius Syndrome Mononeuropathy Motion Sickness Mouth Disease Mucopolysaccharidosis, Type Vii Mucositis Muenke Syndrome Multicentric Castleman Disease Multiple Acyl-Coa Dehydrogenase Deficiency Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Personality Disorder Multiple Sclerosis Multiple System Atrophy 1 Mumps Mungan Syndrome Muscular Atrophy Muscular Dystrophy Muscular Dystrophy, Duchenne Type Mycobacterium Abscessus Mycosis Fungoides Myelodysplastic Syndrome Myeloid Leukemia Myeloma, Multiple Myocardial Infarction Myoclonic Epilepsy Myopathy Sensory Ataxia Myoclonus, Familial Cortical Myotonic Dystrophy Myxozoa Narcissistic Personality Disorder Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Nephrosclerosis Nephrotic Syndrome Neuroblastoma Neuroendocrine Tumor Neuroma Neuronitis Neuropathy Neutropenia Neutrophilic Dermatosis, Acute Febrile Nevus Comedonicus Nijmegen Breakage Syndrome Nodding Syndrome Nodular Lymphocyte Predominant Hodgkin Lymphoma Noonan Syndrome 1 Obsessive-Compulsive Personality Disorder Occipital Horn Syndrome Oligospermia Onchocerciasis Opitz Gbbb Syndrome, Type I Optic Atrophy 1 Orchitis Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteoglophonic Dysplasia Osteomyelitis Osteonecrosis Osteoporotic Fracture Otitis Media Ovalocytosis, Southeast Asian Ovarian Cancer Overhydrated Hereditary Stomatocytosis Pachyonychia Congenita 3 Paine Syndrome Pallister-Hall Syndrome Pancreatic Cancer Pancreatic Neuroendocrine Tumor Pancreatitis Pancreatitis, Hereditary Panic Disorder Papillary Carcinoma Papillomatosis, Confluent and Reticulated Paraneoplastic Pemphigus Paranoid Schizophrenia Patellofemoral Pain Syndrome Patent Foramen Ovale Pathological Gambling Pdgfrb-Associated Chronic Eosinophilic Leukemia Pemphigus Periodontitis Peripheral T-Cell Lymphoma Peritonitis Pernicious Anemia Personality Disorder Pertussis Pervasive Developmental Disorder Phaeohyphomycosis Pheochromocytoma Physical Disorder Pilocytic Astrocytoma Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities Pitt-Hopkins Syndrome Pituitary Adenoma Placental Choriocarcinoma Plasma Cell Leukemia Plasmodium Falciparum Malaria Pneumonia Pneumothorax Pneumothorax, Primary Spontaneous Poikiloderma, Hereditary Fibrosing, with Tendon Contractures, Myopathy, and Pulmonary Fibrosis Polydactyly Polydactyly, Preaxial I Polykaryocytosis Inducer Polymorphic Reticulosis Polyradiculoneuropathy Porphyria Variegata Posterior Myocardial Infarction Posterolateral Myocardial Infarction Postpartum Depression Post-Traumatic Stress Disorder Postural Hypotension Potocki-Shaffer Syndrome Pre-Eclampsia Premature Chromatid Separation Trait Premature Ejaculation Prieto X-Linked Mental Retardation Syndrome Primary Bone Lymphoma Primary Central Nervous System Lymphoma Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type Primary Mediastinal Large B-Cell Lymphoma Proctitis Progressive Familial Heart Block, Type Ib Prolymphocytic Leukemia Prostate Cancer Prostatic Hyperplasia, Benign Prostatitis Psoriasis Psoriasis 13 Psoriasis 2 Psoriasis 7 Psychotic Disorder Pulmonary Fibrosis Pulmonary Hypertension, Primary, 2 Pure Red-Cell Aplasia Purpura Pyruvate Kinase Deficiency of Red Cells Radiation Proctitis Rapp-Hodgkin Syndrome Recurrent Respiratory Papillomatosis Relapsing-Remitting Multiple Sclerosis Renovascular Hypertension Respiratory Distress Syndrome in Premature Infants Reticulosarcoma Retinitis Retinoblastoma Retinoschisis 1, X-Linked, Juvenile Reye Syndrome Rhabdomyosarcoma Rheumatic Fever Rheumatic Fever-Related Antigen Rheumatoid Arthritis Rhinitis Rift Valley Fever Right Bundle Branch Block Ring Chromosome 10 Ring Chromosome 11 Ring Chromosome 13 Ring Chromosome 15 Ring Chromosome 18 Ring Chromosome 2 Ring Chromosome 20 Ring Chromosome 22 Ring Chromosome 3 Ring Chromosome 4 Ring Chromosome 8 Ring Chromosome 9 Sacrococcygeal Teratoma Sarcoidosis 2 Sarcoma Scarlet Fever Schizoaffective Disorder Schizophrenia Schizophreniform Disorder Schizotypal Personality Disorder Seminoma Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Severe Acute Respiratory Syndrome Severe Combined Immunodeficiency Shigellosis Sialadenitis Sick Sinus Syndrome Silver-Russell Syndrome Silver-Russell Syndrome Due to Maternal Uniparental Disomy of Chromosome 7 Sinusitis Situs Inversus Skin/hair/eye Pigmentation, Variation in, 1 Smith-Kingsmore Syndrome Smoking As a Quantitative Trait Locus 3 Social Phobia Somatization Disorder Spastic Cerebral Palsy Spasticity Spastic Paraparesis Spinal Muscular Atrophy Spinal Stenosis Spindle Cell Hemangioma Spinocerebellar Ataxia 10 Splenic Marginal Zone Lymphoma Spondylocarpotarsal Synostosis Syndrome Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations Spondyloocular Syndrome Spotted Fever Squamous Cell Carcinoma Status Epilepticus Streptococcal Meningitis Substance Dependence Synovitis Systemic Lupus Erythematosus T-Cell Leukemia Teratoma Testicular Regression Syndrome Testicular Seminoma Testicular Torsion Tetraploidy Thalassemia Thrombasthenia Thrombocytopenia Thrombosis Thymoma Thyroid Cancer Thyroid Cancer, Nonmedullary, 1 Thyroiditis Thyroid Lymphoma Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Tooth Disease Toxic Oil Syndrome Tracheobronchomalacia Transcobalamin I Deficiency Transitional Cell Carcinoma Transmitted_by Transsexualism Transsexuality Traumatic Brain Injury Tremor Trichomoniasis Tuberous Sclerosis 1 Tuberous Sclerosis 2 Turner Syndrome Typhoid Fever Ulcerative Colitis Ureteral Obstruction Ureterocele Urethral Stricture Urethritis Urinary Tract Obstruction Uruguay Faciocardiomusculoskeletal Syndrome Uterine Sarcoma Uveitis Vaccinia Vaginitis Van Der Woude Syndrome 1 Vascular Dementia Vascular Disease Virus-Associated Trichodysplasia Spinulosa Visceral Leishmaniasis Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Von Hippel-Lindau Syndrome Wandering Spleen Whiplash Wild Type Attr Amyloidosis Wiskott-Aldrich Syndrome Witkop Syndrome Wolff-Parkinson-White Syndrome