Informaţii despre

Nume Noonan Syndrome 1
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Congenital malformation syndromes predominantly associated with short stature
Clasificare anatomică Malacards Boli ale ochiului; Boli ale sistemului reproducator; Boli cardiovasculare; Boli de piele; Boli endocrine; Boli nefrologice (ale rinichilor); Boli neuronale
Boli din aceeaşi familie Noonan Syndrome 10; Noonan Syndrome 2; Noonan Syndrome 3; Noonan Syndrome 4; Noonan Syndrome 5; Noonan Syndrome 6; Noonan Syndrome 7; Noonan Syndrome 8; Noonan Syndrome 9

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Boli A-Z 47,xyy Acid-Labile Subunit Deficiency Acneiform Dermatitis Acquired Von Willebrand Syndrome Acromegaly Acromesomelic Dysplasia Acromesomelic Dysplasia, Maroteaux Type Adenoid Hypertrophy Adenoiditis Adie Pupil Aging Albinism Alexithymia 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 Aneurysm Angiodysplasia Angiokeratoma Aniridia 1 Anorexia Nervosa 1 Anterior Uveitis Antiphospholipid Syndrome Aortic Coarctation Aortitis Arachnoiditis Arteries, Anomalies of Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Astrocytoma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrial Standstill 1 Autoimmune Disease Autosomal Dominant Café Au Lait Spots Baraitser-Winter Syndrome Baraitser-Winter Syndrome 1 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Branchiootic Syndrome 1 Breast Juvenile Papillomatosis Breast Papillomatosis Burkitt Lymphoma Capillary Malformation-Arteriovenous Malformation Capillary Malformations, Congenital Cardiac Tamponade Cardiofaciocutaneous Syndrome 1 Cataract Cavernous Hemangioma Cerebritis Cervicitis Charcot-Marie-Tooth Disease Cherubism Chiari Malformation Childhood Leukemia Choriocarcinoma of Ovary Chromosomal Triplication Chronic Myelomonocytic Leukemia Chylothorax, Congenital Cognitive Function 1, Social Colorectal Adenoma Complete Atrioventricular Canal Congenital Ichthyosiform Erythroderma Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi Constrictive Pericarditis Core Binding Factor Acute Myeloid Leukemia Costello Syndrome Craniosynostosis Cutis Verticis Gyrata Cyanosis, Transient Neonatal Diffuse Idiopathic Skeletal Hyperostosis Dwarfism Embryonal Rhabdomyosarcoma Endocarditis Endometriosis Endotheliitis Factor Xi Deficiency Fanconi Anemia, Complementation Group E Focal Segmental Glomerulosclerosis Gastroenteritis Giant Cell Reparative Granuloma Granular Cell Tumor Growth Control, Y-Chromosome Influenced Growth Hormone Deficiency Hashimoto Thyroiditis Hemangioma Hepatic Adenomas, Familial Hepatoblastoma Hydrocephalus Hydrops Fetalis Hydrops Fetalis, Nonimmune Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperpituitarism Hypertelorism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Hypoplastic Left Heart Syndrome Infective Endocarditis Intermittent Claudication Isolated Growth Hormone Deficiency, Type Ib Juvenile Myelomonocytic Leukemia Kawasaki Disease Keloid Formation Keloids Keratoconus Keratosis Keratosis Pilaris Atrophicans Laron Syndrome Legius Syndrome Lentigines Leopard Syndrome Leukemia Lipomatosis Liver Angiosarcoma Liver Disease Lung Benign Neoplasm Lung Cancer Lung Cancer Susceptibility 3 Lupus Erythematosus Lymphangiectasia, Intestinal Lymphangiectasis Lymphangioma Lymphangiomatosis Lymphatic Malformations Lymphedema Lymphedema, Hereditary, Ii Lymphoblastic Leukemia Lymphoma Malignant Conjunctival Melanoma Mature Cataract Mediastinitis Melanoma Meningitis Microcystic Lymphatic Malformation Moyamoya Disease 1 Multiple Pterygium Syndrome, Escobar Variant Muscular Dystrophy Myelodysplastic Myeloproliferative Cancer Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Neuroblastoma Neurofibroma Neurofibromatosis-Noonan Syndrome Neurofibromatosis, Type I Neurofibromatosis, Type Iv, of Riccardi Neuropathy Nevus, Epidermal Noonan-Like/multiple Giant Cell Lesion Syndrome Noonan Syndrome 2 Noonan Syndrome-Like Disorder with Loose Anagen Hair 1 Noonan Syndrome with Multiple Lentigines Ocular Albinism Orbit Rhabdomyosarcoma Ovarian Melanoma Paronychia Parotitis Partial Atrioventricular Canal Patent Foramen Ovale Pdgfrb-Associated Chronic Eosinophilic Leukemia Pericarditis Pigmented Villonodular Synovitis Pilocytic Astrocytoma Pilomyxoid Astrocytoma Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities Polydactyly Polykaryocytosis Inducer Propionic Acidemia Protein-Losing Enteropathy Pseudo-Turner Syndrome Psoriasis Psoriasis 13 Ptosis Pulmonary Interstitial Glycogenosis Pulmonary Supravalvular Stenosis Pulmonary Valve Disease Pulmonary Valve Stenosis Pulmonic Stenosis Pustular Psoriasis Retinal Detachment Retinitis Retinitis Pigmentosa Rhabdomyosarcoma Rhabdomyosarcoma, Embryonal, 1 Rheumatic Fever Rheumatic Fever-Related Antigen Sarcoma Schimmelpenning-Feuerstein-Mims Syndrome Secondary Adrenal Insufficiency Short-Rib Thoracic Dysplasia 10 with or Without Polydactyly Short-Rib Thoracic Dysplasia 3 with or Without Polydactyly Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sigmoid Neoplasm Silver-Russell Syndrome Sleep Apnea Slipped Capital Femoral Epiphysis Spastic Ataxia, Charlevoix-Saguenay Type Streptococcal Toxic-Shock Syndrome Swyer-James Syndrome Synovitis Systemic Lupus Erythematosus Testicular Trophoblastic Tumor Tetralogy of Fallot Three M Syndrome 1 Thrombocytopenia Thyroid Cancer Thyroiditis Tooth Disease Toxic Shock Syndrome Trophoblastic Neoplasm Tumor Suppressor Gene on Chromosome 11 Turner Syndrome Undifferentiated Pleomorphic Sarcoma Uveitis Vaginitis Villonodular Synovitis Vulvar Angiokeratoma Vulvar Melanoma Watson Syndrome