Informaţii despre

Nume Pseudo-Turner Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificare anatomică Malacards Boli ale ochiului; Boli ale sistemului reproducator; Boli endocrine; Boli nefrologice (ale rinichilor); Boli neuronale
Boli din aceeaşi familie Turner Syndrome Due to Structural X Chromosome Anomalies

Vezi şi

Boli A-Z 47,xyy Acquired Von Willebrand Syndrome Adenoid Hypertrophy Adenoiditis Aging Albinism Alexithymia Alopecia Universalis Congenita Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Aneurysm Angiodysplasia Angiokeratoma Aniridia 1 Anorexia Nervosa 1 Anterior Uveitis Antiphospholipid Syndrome Aortic Coarctation Aortitis Arachnoiditis Arteries, Anomalies of Arthrochalasia Ehlers-Danlos Syndrome Astrocytoma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autoimmune Disease Baraitser-Winter Syndrome Baraitser-Winter Syndrome 1 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Breast Juvenile Papillomatosis Breast Papillomatosis Burkitt Lymphoma Capillary Malformations, Congenital Cardiac Tamponade Cardiofaciocutaneous Syndrome 1 Cataract Cavernous Hemangioma Cerebritis Cervicitis Charcot-Marie-Tooth Disease Cherubism Chiari Malformation Childhood Leukemia Chromosomal Triplication Chronic Myelomonocytic Leukemia Cognitive Function 1, Social Complete Atrioventricular Canal Congenital Ichthyosiform Erythroderma Constrictive Pericarditis Costello Syndrome Craniosynostosis Cutis Verticis Gyrata Cyanosis, Transient Neonatal Dwarfism Embryonal Rhabdomyosarcoma Endocarditis Endometriosis Endotheliitis Factor Xi Deficiency Fanconi Anemia, Complementation Group E Focal Segmental Glomerulosclerosis Gastroenteritis Granular Cell Tumor Growth Hormone Deficiency Hashimoto Thyroiditis Hemangioma Hepatoblastoma Hydrocephalus Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypertelorism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Hypoplastic Left Heart Syndrome Infective Endocarditis Intermittent Claudication Juvenile Myelomonocytic Leukemia Kawasaki Disease Keloid Formation Keloids Keratoconus Keratosis Keratosis Pilaris Atrophicans Lentigines Leopard Syndrome Leukemia Lipomatosis Liver Disease Lupus Erythematosus Lymphangiectasia, Intestinal Lymphangiectasis Lymphangioma Lymphangiomatosis Lymphatic Malformations Lymphedema Lymphoblastic Leukemia Lymphoma Mature Cataract Mediastinitis Meningitis Microcystic Lymphatic Malformation Moyamoya Disease 1 Muscular Dystrophy Myelofibrosis Myeloid Leukemia Neuroblastoma Neurofibroma Neurofibromatosis-Noonan Syndrome Neurofibromatosis, Type I Neurofibromatosis, Type Iv, of Riccardi Neuropathy Noonan-Like/multiple Giant Cell Lesion Syndrome Noonan Syndrome 1 Noonan Syndrome 2 Noonan Syndrome-Like Disorder with Loose Anagen Hair 1 Noonan Syndrome with Multiple Lentigines Ocular Albinism Orbit Rhabdomyosarcoma Parotitis Partial Atrioventricular Canal Patent Foramen Ovale Pdgfrb-Associated Chronic Eosinophilic Leukemia Pericarditis Pigmented Villonodular Synovitis Pilocytic Astrocytoma Pilomyxoid Astrocytoma Polydactyly Polykaryocytosis Inducer Propionic Acidemia Protein-Losing Enteropathy Psoriasis Psoriasis 13 Ptosis Pulmonary Interstitial Glycogenosis Pulmonary Supravalvular Stenosis Pulmonic Stenosis Pustular Psoriasis Retinal Detachment Retinitis Retinitis Pigmentosa Rhabdomyosarcoma Rhabdomyosarcoma, Embryonal, 1 Rheumatic Fever Rheumatic Fever-Related Antigen Short-Rib Thoracic Dysplasia 10 with or Without Polydactyly Short-Rib Thoracic Dysplasia 3 with or Without Polydactyly Sleep Apnea Spastic Ataxia, Charlevoix-Saguenay Type Streptococcal Toxic-Shock Syndrome Swyer-James Syndrome Synovitis Systemic Lupus Erythematosus Tetralogy of Fallot Three M Syndrome 1 Thrombocytopenia Thyroiditis Tooth Disease Toxic Shock Syndrome Turner Syndrome Turner Syndrome Due to Structural X Chromosome Anomalies Uveitis Vaginitis Villonodular Synovitis Vulvar Angiokeratoma Watson Syndrome