Informaţii despre

Nume Turner Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Karyotype 45,X; Karyotype 46,X iso (Xq); Karyotype 46,X with abnormal sex chromosome, except iso (Xq); Mosaicism, 45,X/46,XX or XY; Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome; Other variants of Turner syndrome; Turner syndrome, unspecified
Clasificare anatomică Malacards Boli ale ochiului; Boli ale sistemului reproducator; Boli endocrine; Boli nefrologice (ale rinichilor); Boli neuronale
Boli din aceeaşi familie Pseudo-Turner Syndrome; Turner Syndrome Due to Structural X Chromosome Anomalies

Vezi şi

Boli A-Z 46 Xy Gonadal Dysgenesis 47, Xxy 47,xyy Achalasia Acid-Labile Subunit Deficiency Acrodysostosis Acromegaly Adenocarcinoma Adenoma Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency Aging Alexithymia Alopecia Alopecia Areata 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 Amenorrhea Androgen Insensitivity Syndrome, Mild Aneurysm Angioid Streaks Angiokeratoma Aniridia 1 Anorexia Nervosa 1 Anus, Imperforate Aortic Aneurysm Aortic Coarctation Aplastic Anemia Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Asthma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Attention Deficit-Hyperactivity Disorder Autoimmune Disease Autoimmune Polyendocrine Syndrome Axenfeld-Rieger Syndrome Basal Cell Carcinoma Bipolar Disorder Blastoma Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System 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 Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brachydactyly Breast Disease Bulimia Nervosa 2 Burns Capillary Malformations, Congenital Carotid Artery Dissection Castleman Disease Cataract Celiac Disease 1 Cerebellar Atrophy, Developmental Delay, and Seizures Cerebral Hemorrhage Cerebritis Cervical Aortic Arch Cervicitis Chondrodysplasia Punctata Syndrome Chromosomal Triplication Chromosome 10p Duplication Chromosome 2q Deletion Chromosome Xp Deletion Coats Disease Cognitive Function 1, Social Colitis Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complete Androgen Insensitivity Syndrome Cornelia De Lange Syndrome Coronary Artery Anomaly Costello Syndrome Craniopharyngioma Cutis Verticis Gyrata Cystadenoma Cystic Fibrosis Dandy-Walker Syndrome Diabetes Insipidus Diabetes Mellitus Diabetic Cataract Diffuse Idiopathic Skeletal Hyperostosis Dilated Cardiomyopathy Down Syndrome Dwarfism Dyscalculia Dystonia Embryonal Carcinoma Encephalitis Endemic Goiter Endotheliitis Epilepsy Epithelial Recurrent Erosion Dystrophy Fabry Disease Familial Hypopituitarism Familial Thyroid Dyshormonogenesis Fanconi Anemia, Complementation Group E Fibrous Dysplasia Fox-Fordyce Disease Fragile X Syndrome Ganglioglioma Ganglioneuroblastoma Ganglioneuroma Gastroschisis Gestational Diabetes Gigantism Gilles De La Tourette Syndrome Glioblastoma Glioblastoma Multiforme Glucose Intolerance Goiter Goiter, Multinodular 1, with or Without Sertoli-Leydig Cell Tumors Gonadal Disease Gonadal Dysgenesis Gonadoblastoma Graves' Disease Growth Control, Y-Chromosome Influenced Growth Hormone Deficiency Hair Whorl Halo Nevi Hashimoto Thyroiditis Hemophilia Hemophilia a Hepatitis Hepatitis E Hepatocellular Carcinoma Hermaphroditism Histiocytosis Horseshoe Kidney Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperandrogenism Hyperinsulinism Hyperparathyroidism Hyperpituitarism Hyperproinsulinemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypoadrenalism Hypochondroplasia Hypoglycemia Hypogonadism Hypopituitarism Hypoplastic Left Heart Syndrome Hypothyroidism Hypothyroidism, Congenital, Nongoitrous, 4 Infertility Inflammatory Bowel Disease Insulin-Like Growth Factor I Insulinoma Isolated Growth Hormone Deficiency Isolated Growth Hormone Deficiency, Type Ib Isolated Growth Hormone Deficiency, Type Ii Klippel-Feil Syndrome Langerhans Cell Histiocytosis Langer Mesomelic Dysplasia Laron Syndrome Learning Disability Leber Hereditary Optic Neuropathy Leiomyosarcoma Leri-Weill Dyschondrosteosis Leukemia Lichen Planus Lichen Sclerosus Limbal Stem Cell Deficiency Lupus Erythematosus Lutheran Suppressor, X-Linked Lyme Disease Lymphedema Marasmus Marfan Syndrome Mccune-Albright Syndrome Meningioma, Familial Middle Ear Disease Mixed Gonadal Dysgenesis Monocytic Leukemia Mosaic Variegated Aneuploidy Syndrome 1 Multicentric Castleman Disease Multicystic Dysplastic Kidney Multiple Epiphyseal Dysplasia Mungan Syndrome Muscle Cancer Myasthenia Gravis Myoclonic Epilepsy of Lafora Myxedema Neonatal Hypothyroidism Neuritis Neurofibromatosis, Type Iv, of Riccardi Neuronal Migration Disorders Neuronitis Neuropathy Nondisjunction Non-Functioning Pituitary Adenoma Nontoxic Goiter Noonan Syndrome 1 Norrie Disease Nutritional Deficiency Disease Omenn Syndrome Omphalocele Opitz Gbbb Syndrome, Type I Orofaciodigital Syndrome Viii Osteitis Fibrosa Osteogenesis Imperfecta, Type I Osteonecrosis Osteoporosis, Juvenile Otitis Media Ovarian Disease Paine Syndrome Pancreatitis Papilledema Parsonage Turner Syndrome Partial Deletion of Y Patau Syndrome Pernicious Anemia Persistent Hyperplastic Primary Vitreous Pharyngitis Pilomatrixoma Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities Pituitary Adenoma 1, Multiple Types Pituitary Hormone Deficiency, Combined, 2 Plummer's Disease Polycystic Ovary Syndrome Polyhydramnios Polymicrogyria Portal Vein Thrombosis Precocious Puberty Premature Menopause Premature Ovarian Failure 7 Primary Ciliary Dyskinesia Pseudoainhum Pseudohermaphroditism Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ia Psoriasis Psoriasis 13 Pulmonary Arteriovenous Malformation Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pustular Psoriasis Radiculopathy Ramer Ladda Syndrome Renal Dysplasia, Cystic Retinal Detachment Retinitis Rhabdoid Meningioma Rickets Schizophrenia Scoliosis Secondary Adrenal Insufficiency Severe Hemophilia a Silver-Russell Syndrome Sitosterolemia Situs Inversus Skin Disease Slipped Capital Femoral Epiphysis Squamous Cell Carcinoma Subacute Lymphocytic Thyroiditis Subacute Thyroiditis Subclavian Artery Aneurysm Sympathetic Ophthalmia Systemic Lupus Erythematosus Testicular Cancer Testicular Seminoma Three M Syndrome 1 Thrombosis Thyroid Hormone Resistance, Generalized, Autosomal Dominant Thyroiditis Timothy Syndrome Transitional Cell Carcinoma Triple X Syndrome Triploidy Tuberous Sclerosis Tuberous Sclerosis 1 Tuberous Sclerosis 2 Ulcerative Colitis Velocardiofacial Syndrome Ventricular Fibrillation, Paroxysmal Familial, 1 Virus-Associated Trichodysplasia Spinulosa Wilson-Turner X-Linked Mental Retardation Syndrome X-Linked Chondrodysplasia Punctata