Informaţii despre

Nume Diaphragmatic Hernia, Congenital
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Congenital diaphragmatic hernia; Diaphragmatic hernia with gangrene; Diaphragmatic hernia with obstruction, without gangrene; Diaphragmatic hernia without obstruction or gangrene
Clasificare anatomică Malacards Boli gastrointestinale; Boli musculare; Boli respiratorii
Boli din aceeaşi familie Diaphragmatic Hernia 2; Diaphragmatic Hernia 3

Vezi şi

Boli A-Z 46,xy Partial Gonadal Dysgenesis 46,xy Sex Reversal 1 46,xy Sex Reversal 3 Abdominal Wall Defect Acid-Labile Subunit Deficiency Adenocarcinoma Adenomatoid Tumor Aging Albinism Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Anencephaly Aniridia 1 Anorexia Nervosa 1 Apert Syndrome Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrioventricular Septal Defect Ayme-Gripp Syndrome Azygos Continuation of the Inferior Vena Cava Blood Group--Ahonen Blood Group, I System Brain Injury Brittle Bone Disorder Cardiac Tamponade Carotid Artery Occlusion Cerebritis Cervicitis Charge Syndrome Chromosomal Triplication Chromosome 11q Duplication Chromosome 15q24 Deletion Syndrome Chromosome 16p Duplication Chromosome 16 Trisomy Chromosome 2q35 Duplication Syndrome Complete Atrioventricular Canal-Left Heart Obstruction Syndrome Complete Atrioventricular Canal-Tetralogy of Fallot Syndrome Complete Atrioventricular Canal-Ventricle Hypoplasia Syndrome Congenital Bronchobiliary Fistula Conotruncal Heart Malformations Cornelia De Lange Syndrome Craniofacial-Deafness-Hand Syndrome Craniofrontonasal Syndrome Craniorachischisis Cryptophthalmos Cystic Fibrosis Denys-Drash Syndrome Developmental Dysplasia of the Hip 1 Diabetes Mellitus Diaphragmatic Eventration Diaphragmatic Hernia 2 Diaphragmatic Hernia 3 Diaphragm Disease Duodenal Atresia Duodenal Obstruction Duodenitis Ehlers-Danlos Syndrome Emanuel Syndrome Encephalopathy Endotheliitis Enterocele Esophageal Atresia Esophageal Atresia/tracheoesophageal Fistula Exencephaly Fraser Syndrome 1 Fryns Syndrome Gastroesophageal Reflux Gastroschisis Heart Septal Defect Heavy Chain Disease Hemangioendothelioma Hemangioma of Lung Hepatic Adenomas, Familial Hepatitis Hereditary Wilms' Tumor Hernia, Anterior Diaphragmatic Hernia, Hiatus Hydrocele Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hyperphosphatasia-Intellectual Disability Syndrome Hyperphosphatasia with Mental Retardation Syndrome 1 Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Pyloric Stenosis Hypoplastic Left Heart Syndrome Hypoxia Interstitial Emphysema Interstitial Lung Disease Intestinal Perforation Intestinal Volvulus Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies Limb Reduction Defect Lung Agenesis Lung Disease Macrophagic Myofasciitis Meacham Syndrome Mediastinitis Microphthalmia Microphthalmia, Syndromic 9 Microtia Muenke Syndrome Myelomeningocele Myopathy Nance-Horan Syndrome Nasopharyngeal Teratoma Nasopharyngitis Nemaline Myopathy Neonatal Diabetes Mellitus Neonatal Respiratory Failure Neural Tube Defects Neural Tube Defects, Folate-Sensitive Newborn Respiratory Distress Syndrome Obstructive Jaundice Oligohydramnios Omphalocele Ovarian Germ Cell Cancer Pallister-Killian Mosaic Syndrome Pallister-Killian Syndrome Pancreatic Agenesis Pancreatitis Partial Atrioventricular Canal Patau Syndrome Patent Foramen Ovale Pericardial Effusion Peritoneal Serous Adenocarcinoma Peritoneal Serous Papillary Adenocarcinoma Peritonitis Pleuropneumonia Pneumonia Pneumothorax Polyhydramnios Premature Ovarian Failure 7 Pulmonary Alveolar Proteinosis Pulmonary Hypertension Pulmonary Immaturity Pulmonary Sclerosing Hemangioma Pulmonary Sequestration Pyloric Stenosis Renal Agenesis, Unilateral Renal Hypodysplasia/aplasia 1 Respiratory Distress Syndrome in Premature Infants Respiratory Failure Saal Bulas Syndrome Sacrococcygeal Teratoma Sarcomatoid Mesothelioma Scoliosis Simpson-Golabi-Behmel Syndrome Situs Inversus Smith-Magenis Syndrome Spastic Ataxia, Charlevoix-Saguenay Type Splenic Infarction Surfactant Dysfunction Teratoma Tetralogy of Fallot Tetrasomy 9p Thyroiditis Total Anomalous Pulmonary Venous Return 1 Tracheobronchomegaly Tracheoesophageal Fistula Transposition of the Great Arteries Trisomy 22 Vacterl Association Ventricular Septal Defect Wandering Spleen Witteveen-Kolk Syndrome Wolf-Hirschhorn Syndrome