Omphalocele

Informaţii despre

Nume		Omphalocele
Pagina Web		www.malacards.org
Clasificare globală Malacards		Boli fetale; Boli rare
Clasificari ICD10		Exomphalos
Boli din aceeaşi familie		Omphalocele, Autosomal

Vezi şi

Boli A-Z		Abdominal Wall Defect Acrocallosal Syndrome Aging Agnathia-Microstomia-Synotia Alobar Holoprosencephaly Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alveolar Capillary Dysplasia Anencephaly Aniridia 1 Anorexia Nervosa 1 Anuria Apert Syndrome Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Atrial Septal Defect Coronary Sinus Ayme-Gripp Syndrome Azoospermia Beckwith-Wiedemann Syndrome Biliary Atresia Blood Group--Ahonen Blood Group, I System Boomerang Dysplasia Brachial Amelia, Cleft Lip, and Holoprosencephaly Budd-Chiari Syndrome Cardiac Diverticulum Cat Eye Syndrome Chromosomal Triplication Chromosome 3q Duplication Cleft Lip Cloacal Exstrophy Coarctation of Aorta Colonic Atresia Cornelia De Lange Syndrome Cor Triatriatum Craniorachischisis Craniosynostosis Cystic Teratoma Dextrocardia Diaphragmatic Hernia, Congenital Diploid-Triploid Mosaicism Double Discordia Down Syndrome Duodenal Atresia Duodenal Obstruction Duodenitis Dwarfism Dysostosis Ectopia Cordis Encephalocele Esophageal Atresia Exencephaly Exstrophy of Bladder Fanconi Anemia, Complementation Group E Fibrodysplasia Ossificans Progressiva Focal Dermal Hypoplasia Gastroschisis Germ Cell and Embryonal Cancer Hemangioma Hemihyperplasia, Isolated Hepatic Adenomas, Familial Hepatitis Hernia, Hiatus Holoprosencephaly Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoglycemia Hypoplastic Left Heart Syndrome Hypospadias Inguinal Hernia Intestinal Atresia Ischemia Jejunal Atresia Laryngitis Learning Disability Limb-Body Wall Complex Macroglossia Medulloblastoma Melnick-Needles Syndrome Mercury Poisoning Multiple Pterygium Syndrome, Lethal Type Nail-Patella Syndrome Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neurodegeneration with Brain Iron Accumulation 2a Oeis Complex Omphalocele-Cleft Palate Syndrome, Lethal Omphalocele-Diaphragmatic Hernia-Cardiovascular Anomalies-Radial Ray Defect Syndrome Omphalocele, Exstrophy of the Cloaca, Imperforate Anus, and Spinal Defects Complex Orbital Cyst Orofacial Cleft Orofaciodigital Syndrome Viii Otopalatodigital Syndrome Otopalatodigital Syndrome, Type Ii Pentalogy of Cantrell Pericardial Effusion Pericarditis Persistent Idiopathic Facial Pain Pharyngitis Physical Disorder Placental Choriocarcinoma Polydactyly Polyhydramnios Prune Belly Syndrome Pulmonary Hypertension Sacral Defect with Anterior Meningocele Sacrococcygeal Teratoma Scoliosis Shprintzen Omphalocele Syndrome Sirenomelia Spastic Ataxia, Charlevoix-Saguenay Type Spastic Paraplegia 17, Autosomal Dominant Synpolydactyly Teratoma Tetralogy of Fallot Thoracoabdominal Syndrome Three M Syndrome 1 Thyroiditis Transposition of the Great Arteries Trisomy 1q Turner Syndrome Vaginitis Ventricular Fibrillation, Paroxysmal Familial, 1 Ventricular Septal Defect Vitamin Metabolic Disorder Wandering Spleen