CDH
MCID: DPH024
MIFTS: 66

Diaphragmatic Hernia, Congenital (CDH)

Categories: Fetal diseases, Gastrointestinal diseases, Genetic diseases, Muscle diseases, Rare diseases, Respiratory diseases

Aliases & Classifications for Diaphragmatic Hernia, Congenital

MalaCards integrated aliases for Diaphragmatic Hernia, Congenital:

Name: Diaphragmatic Hernia, Congenital 57 75
Congenital Diaphragmatic Hernia 12 75 24 53 25 59 37 29 6 15 17 33
Diaphragmatic Hernia 12 15 17 33
Hernia, Congenital Diaphragmatic 1 57 13
Congenital Diaphragmatic Defect 53 25
Hernia, Diaphragmatic 44 40
Cdh 53 59
Hernia, Congenital Diaphragmatic; Hcd; Cdh 57
Diaphragm, Unilateral Agenesis of 57
Hernia, Congenital Diaphragmatic 57
Diaphragmatic Defect, Congenital 57
Unilateral Agenesis of Diaphragm 53
Hernia Diaphragmatic Congenital 55
Hemidiaphragm, Agenesis of 57
Agenesis of Hemidiaphragm 53
Hernia Diaphragmatic 55
Dih 57
Hcd 57

Characteristics:

Orphanet epidemiological data:

59
congenital diaphragmatic hernia
Inheritance: Multigenic/multifactorial,Not applicable; Prevalence: 1-5/10000 (Worldwide),1-5/10000 (Europe),1-5/10000 (Austria),1-5/10000 (Belgium),1-5/10000 (Croatia),1-5/10000 (Denmark),1-5/10000 (France),1-9/100000 (Germany),1-5/10000 (Hungary),1-5/10000 (Ireland),1-5/10000 (Italy),1-5/10000 (Malta),1-5/10000 (Netherlands),1-5/10000 (Norway),1-9/100000 (Poland),1-5/10000 (Portugal),1-9/100000 (Spain),1-5/10000 (Switzerland),1-5/10000 (United Kingdom),1-5/10000 (Ukraine); Age of onset: Neonatal; Age of death: early childhood;

OMIM:

57
Inheritance:
multifactorial
? some autosomal recessive cases


HPO:

32
diaphragmatic hernia, congenital:
Inheritance multifactorial inheritance


Classifications:



External Ids:

Disease Ontology 12 DOID:3827
OMIM 57 142340
KEGG 37 H01241
MeSH 44 D006548
NCIt 50 C34687
SNOMED-CT 68 39839004
MESH via Orphanet 45 C538080
ICD10 via Orphanet 34 Q79.0
UMLS via Orphanet 73 C0235833
Orphanet 59 ORPHA2140
MedGen 42 C0235833
UMLS 72 C0019284

Summaries for Diaphragmatic Hernia, Congenital

Genetics Home Reference : 25 Congenital diaphragmatic hernia is a defect in the diaphragm. The diaphragm, which is composed of muscle and other fibrous tissue, separates the organs in the abdomen from those in the chest. Abnormal development of the diaphragm before birth leads to defects ranging from a thinned area in the diaphragm to its complete absence. An absent or partially formed diaphragm results in an abnormal opening (hernia) that allows the stomach and intestines to move into the chest cavity and crowd the heart and lungs. This crowding can lead to underdevelopment of the lungs (pulmonary hypoplasia), potentially resulting in life-threatening breathing difficulties that are apparent from birth. In 5 to 10 percent of affected individuals, signs and symptoms of congenital diaphragmatic hernia appear later in life and may include breathing problems or abdominal pain from protrusion of the intestine into the chest cavity. In about 1 percent of cases, congenital diaphragmatic hernia has no symptoms; it may be detected incidentally when medical imaging is done for other reasons. Congenital diaphragmatic hernias are often classified by their position. A Bochdalek hernia is a defect in the side or back of the diaphragm. Between 80 and 90 percent of congenital diaphragmatic hernias are of this type. A Morgnani hernia is a defect involving the front part of the diaphragm. This type of congenital diaphragmatic hernia, which accounts for approximately 2 percent of cases, is less likely to cause severe symptoms at birth. Other types of congenital diaphragmatic hernia, such as those affecting the central region of the diaphragm, or those in which the diaphragm muscle is absent with only a thin membrane in its place, are rare.

MalaCards based summary : Diaphragmatic Hernia, Congenital, also known as congenital diaphragmatic hernia, is related to microphthalmia, syndromic 9 and double outlet right ventricle. An important gene associated with Diaphragmatic Hernia, Congenital is GATA6 (GATA Binding Protein 6), and among its related pathways/superpathways are Mesodermal Commitment Pathway and Embryonic and Induced Pluripotent Stem Cell Differentiation Pathways and Lineage-specific Markers. The drugs Nitric Oxide and Sodium citrate have been mentioned in the context of this disorder. Affiliated tissues include lung, heart and fetal lung, and related phenotypes are congenital diaphragmatic hernia and respiratory distress

Disease Ontology : 12 A diaphragm disease characterized by the lack of development of all or part of the diaphragm, which results in an abnormal opening that allows the stomach and intestines to move into the chest cavity and crowd the heart and lungs.

NIH Rare Diseases : 53 Congenital diaphragmatic hernia (CDH) is a condition present before birth characterized by abnormal development of the diaphragm. The diaphragm normally separates the organs in the abdomen from those in the chest. The severity of CDH may range from a thinned area in part of the diaphragm, to its complete absence. CDH may allow the stomach and intestines to move through an opening (hernia) into the chest cavity, crowding the heart and lungs. This can then lead to underdevelopment of the lungs (pulmonary hypoplasia), which may cause life-threatening complications. CDH may be associated with several syndromes (some caused by genetic mutations or a chromosome abnormality), it may be associated with other birth defects, or it may occur with no other abnormalities. It is rarely inherited. Treatment options depend on the type and severity of the defect and typically include surgery. Prenatal diagnosis and medical advances have increased the survival rate, but various long-term complications affecting health and development may occur.

OMIM : 57 Congenital diaphragmatic hernia (CDH) refers to a group of congenital defects in the structural integrity of the diaphragm which are often associated with lethal pulmonary hypoplasia and pulmonary hypertension. Prevalence in newborns ranges from 1 in 2,500 to 1 in 4,000, and there is a 30 to 60% mortality rate (Langham et al., 1996; Harrison et al., 1994; Nobuhara et al., 1996). Most cases of congenital diaphragmatic hernia are sporadic. (142340)

KEGG : 37
Congenital diaphragmatic hernia (CDH) is defined as a protrusion of abdominal viscera into the thorax through an abnormal opening or defect that is present at birth. CDH is often associated with potentially lethal lung hypoplasia and pulmonary hypertension. Despite advances in therapy, mortality remains high. Although the etiology of most cases of CDH remains unknown, there is increasing evidence that specific pathways and genes play a role in the development of CDH. It has been reported that a patient who has nonsense mutation in FOG2/ ZFPM2, died at birth with a diaphragmatic defect and severe pulmonary hypoplasia.

Wikipedia : 75 Congenital diaphragmatic hernia (CDH) is a birth defect of the diaphragm. The most common type of CDH is... more...

GeneReviews: NBK1359

Related Diseases for Diaphragmatic Hernia, Congenital

Diseases in the Hernia, Anterior Diaphragmatic family:

Diaphragmatic Hernia, Congenital Diaphragmatic Hernia 2
Diaphragmatic Hernia 3

Diseases related to Diaphragmatic Hernia, Congenital via text searches within MalaCards or GeneCards Suite gene sharing:

(show top 50) (show all 654)
# Related Disease Score Top Affiliating Genes
1 microphthalmia, syndromic 9 34.5 STRA6 FREM2 FGF10
2 double outlet right ventricle 31.4 ZFPM2 GATA6 GATA4
3 fraser syndrome 1 31.2 FREM2 FREM1 FRAS1
4 renal hypodysplasia/aplasia 1 31.1 FREM2 FREM1 FRAS1
5 patent foramen ovale 31.1 NKX2-1 GATA6 GATA4
6 heart septal defect 31.1 ZFPM2 GATA6 GATA4
7 esophageal atresia/tracheoesophageal fistula 31.0 TEF FGF10
8 diaphragmatic eventration 31.0 ZFPM2 TEF STRA6 PAX3
9 donnai-barrow syndrome 30.8 ZFPM2 NR2F2 GATA4
10 ventricular septal defect 30.8 ZFPM2 NR2F2 GATA6 GATA4
11 duodenal atresia 30.8 TEF FGF10
12 chromosome 2q35 duplication syndrome 30.8 GLI3 FREM2 FRAS1
13 omphalocele, diaphragmatic hernia, and radial ray defects 12.6
14 epidermolysis bullosa with diaphragmatic hernia 12.5
15 dandy-walker malformation with nasopharyngeal teratoma and diaphragmatic hernia 12.4
16 diaphragmatic hernia upper limb defects 12.4
17 lethal hydranencephaly-diaphragmatic hernia syndrome 12.4
18 diaphragmatic hernia-short bowel-asplenia syndrome 12.4
19 microphthalmia, syndromic 12 12.3
20 craniofacial-deafness-hand syndrome 12.3
21 developmental dysplasia of the hip 1 12.2
22 tonne-kalscheuer syndrome 12.0
23 cardiac-urogenital syndrome 11.8
24 saal bulas syndrome 11.7
25 multiple pterygium syndrome, escobar variant 11.7
26 chromosome 15q24 deletion syndrome 11.7
27 drug reaction with eosinophilia and systemic symptoms 11.7
28 froster-huch syndrome 11.6
29 heavy chain disease 11.5
30 alpha-heavy chain disease 11.5
31 linear skin defects with multiple congenital anomalies 1 11.5
32 pulmonary hypertension, neonatal 11.4
33 chromosome 8p23.1 deletion 11.4
34 pallister-killian mosaic syndrome 11.4
35 schisis association 11.4
36 diaphragmatic hernia 3 11.4
37 multiple pterygium syndrome, lethal type 11.3
38 gillessen-kaesbach-nishimura syndrome 11.3
39 lowry-maclean syndrome 11.3
40 williams-beuren region duplication syndrome 11.3
41 white-sutton syndrome 11.3
42 iniencephaly 11.3
43 split hand urinary anomalies spina bifida 11.3
44 gamma heavy chain disease 11.2
45 agammaglobulinemia 11.2
46 gastroesophageal reflux 10.8
47 complete atrioventricular canal-left heart obstruction syndrome 10.7 NR2F2 GATA4
48 complete atrioventricular canal-ventricle hypoplasia syndrome 10.7 NR2F2 GATA6 GATA4
49 partial atrioventricular canal 10.7 NR2F2 GATA6 GATA4
50 complete atrioventricular canal-tetralogy of fallot syndrome 10.7 NR2F2 GATA4

Graphical network of the top 20 diseases related to Diaphragmatic Hernia, Congenital:



Diseases related to Diaphragmatic Hernia, Congenital

Symptoms & Phenotypes for Diaphragmatic Hernia, Congenital

Human phenotypes related to Diaphragmatic Hernia, Congenital:

59 32 (show all 8)
# Description HPO Frequency Orphanet Frequency HPO Source Accession
1 congenital diaphragmatic hernia 59 32 hallmark (90%) Very frequent (99-80%) HP:0000776
2 respiratory distress 59 Frequent (79-30%)
3 intestinal malrotation 59 Frequent (79-30%)
4 hypoxemia 59 Frequent (79-30%)
5 pulmonary hypoplasia 59 Frequent (79-30%)
6 abnormality of cardiovascular system morphology 59 Frequent (79-30%)
7 prominent sternum 59 Frequent (79-30%)
8 aplasia/hypoplasia of the diaphragm 59 Frequent (79-30%)

Symptoms via clinical synopsis from OMIM:

57
Thorax:
familial congenital diaphragmatic hernia

Clinical features from OMIM:

142340

MGI Mouse Phenotypes related to Diaphragmatic Hernia, Congenital:

46 (show all 22)
# Description MGI Source Accession Score Top Affiliating Genes
1 cardiovascular system MP:0005385 10.45 FGF10 FRAS1 FREM2 GATA4 GATA6 GLI3
2 mortality/aging MP:0010768 10.4 CDK8 FGF10 FRAS1 FREM1 FREM2 GATA4
3 growth/size/body region MP:0005378 10.37 FGF10 FRAS1 FREM1 FREM2 GATA4 GATA6
4 homeostasis/metabolism MP:0005376 10.33 FGF10 GATA4 GATA6 GLI3 NKX2-1 NR2F2
5 cellular MP:0005384 10.3 FGF10 FRAS1 GATA4 GATA6 GLI3 NKX2-1
6 embryo MP:0005380 10.27 CDK8 FGF10 FREM2 GATA4 GATA6 GLI3
7 endocrine/exocrine gland MP:0005379 10.22 FGF10 FREM1 GATA4 GLI3 NKX2-1 NR2F2
8 nervous system MP:0003631 10.2 FGF10 FREM1 FREM2 GATA4 GLI3 NKX2-1
9 digestive/alimentary MP:0005381 10.19 FGF10 FRAS1 FREM1 GATA4 GLI3 NKX2-1
10 integument MP:0010771 10.19 FGF10 FRAS1 FREM1 FREM2 GATA4 GLI3
11 limbs/digits/tail MP:0005371 10.18 FGF10 FRAS1 FREM1 FREM2 GATA4 GATA6
12 muscle MP:0005369 10.18 FGF10 FREM1 FREM2 GATA4 GATA6 NR2F2
13 craniofacial MP:0005382 10.14 FGF10 FRAS1 FREM1 FREM2 GLI3 PAX3
14 no phenotypic analysis MP:0003012 10.13 FRAS1 GATA4 GLI3 NKX2-1 NR2F2 PAX3
15 normal MP:0002873 10.06 FGF10 FREM1 GATA4 GATA6 GLI3 NKX2-1
16 liver/biliary system MP:0005370 10.05 FREM1 GATA4 GATA6 PAX3 TEF WT1
17 reproductive system MP:0005389 10 FGF10 FREM1 FREM2 GATA4 GATA6 GLI3
18 renal/urinary system MP:0005367 9.92 FGF10 FRAS1 FREM1 FREM2 GLI3 PAX3
19 respiratory system MP:0005388 9.9 FGF10 FRAS1 FREM1 FREM2 GATA4 GATA6
20 pigmentation MP:0001186 9.77 FREM2 GLI3 NR2F2 PAX3 STRA6
21 skeleton MP:0005390 9.61 FGF10 FRAS1 FREM1 FREM2 GATA4 GLI3
22 vision/eye MP:0005391 9.23 FGF10 FRAS1 FREM1 FREM2 GLI3 NR2F2

Drugs & Therapeutics for Diaphragmatic Hernia, Congenital

Drugs for Diaphragmatic Hernia, Congenital (from DrugBank, HMDB, Dgidb, PharmGKB, IUPHAR, NovoSeek, BitterDB):

(show top 50) (show all 114)
# Name Status Phase Clinical Trials Cas Number PubChem Id
1
Nitric Oxide Approved Phase 4 10102-43-9 145068
2
Sodium citrate Approved, Investigational Phase 4 68-04-2
3
Sorbitol Approved Phase 4 50-70-4 5780
4
Tocopherol Approved, Investigational Phase 4 1406-66-2, 54-28-4 14986
5 Coconut Approved Phase 4
6
Citric acid Approved, Nutraceutical, Vet_approved Phase 4 77-92-9 311
7
Vitamin E Approved, Nutraceutical, Vet_approved Phase 4 59-02-9 14985
8 Tocotrienol Investigational Phase 4 6829-55-6
9 Sildenafil Citrate Phase 4 171599-83-0
10 Citrate Phase 4
11 Phosphodiesterase Inhibitors Phase 4
12 Phosphodiesterase 5 Inhibitors Phase 4
13 Vasodilator Agents Phase 4
14 Gastrointestinal Agents Phase 4
15 Olive Phase 4
16 Soy Bean Phase 4
17 Pharmaceutical Solutions Phase 4
18 Fat Emulsions, Intravenous Phase 4
19 Cathartics Phase 4
20 Parenteral Nutrition Solutions Phase 4
21 Tocotrienols Phase 4
22 Tocopherols Phase 4
23 Laxatives Phase 4
24
Omeprazole Approved, Investigational, Vet_approved Phase 3 73590-58-6 4594
25
Midazolam Approved, Illicit Phase 3 59467-70-8 4192
26
Ketamine Approved, Vet_approved Phase 3 6740-88-1 3821
27
Titanium dioxide Approved Phase 3 13463-67-7
28
Aspirin Approved, Vet_approved Phase 3 50-78-2 2244
29
Povidone Approved Phase 3 9003-39-8
30 Anesthetics Phase 3
31 Antacids Phase 3
32 Proton Pump Inhibitors Phase 3
33 Anti-Ulcer Agents Phase 3
34 Anesthetics, Intravenous Phase 3
35 Tranquilizing Agents Phase 3
36 Anti-Anxiety Agents Phase 3
37 GABA Agents Phase 3
38 Adjuvants, Anesthesia Phase 3
39 Hypnotics and Sedatives Phase 3
40 GABA Modulators Phase 3
41 Excitatory Amino Acid Antagonists Phase 3
42 Anesthetics, Dissociative Phase 3
43 Psychotropic Drugs Phase 3
44 Anesthetics, General Phase 3
45 Excitatory Amino Acids Phase 3
46 Acidophilus Phase 3
47 Bifidobacterium Phase 3
48 Peripheral Nervous System Agents Phase 3
49 Protective Agents Phase 3
50 Platelet Aggregation Inhibitors Phase 3

Interventional clinical trials:

(show top 50) (show all 72)
# Name Status NCT ID Phase Drugs
1 Chronic Sildenafil for Severe Diaphragmatic Hernia Terminated NCT00133679 Phase 4 sildenafil;Placebo
2 Incidence and Severity of Parenteral Nutrition Associated Cholestasis in Neonates Subjected to Major Surgery, Using Two Mixed Intravenous Lipid Emulsions Terminated NCT02633384 Phase 4
3 Rectal and Oral Omeprazole Treatment of Gastroesophageal Reflux in Infants With Esophageal Atresia or Congenital Diaphragmatic Hernia; A Pharmacodynamic and Pharmacokinetic Study. Unknown status NCT00226044 Phase 3 Omeprazole suppository
4 Intranasal Midazolam Versus Intranasal Ketamine to Sedate Newborns for Intubation in Delivery Room. Unknown status NCT01517828 Phase 3 Sedation by ketamine;Sedation with Midazolam
5 The Use of Probiotics in the Management of Necrotizing Enterocolitis in HIV-exposed Premature and Very-low Birth Weight Infants Completed NCT01868737 Phase 3
6 Randomized Trial of Fetoscopic Endoluminal Tracheal Occlusion (FETO) Versus Expectant Management During Pregnancy in Fetuses With Left Sided and Isolated Congenital Diaphragma Hernia and Severe Pulmonary Hypoplasia. Recruiting NCT01240057 Phase 2, Phase 3
7 Contribution of PRF (Platelet Rich Fibrin) in the Biological Functionalization of Prothetic Patch Closure : in Vitro Study Not yet recruiting NCT03861182 Phase 3
8 Investigating the Role of Early Low-dose Aspirin in Diabetes: A Phase III Multicentre Double-blinded Placebo-controlled Randomised Trial of Low-dose Aspirin Initiated in the First Trimester of Diabetes Pregnancy Not yet recruiting NCT03574909 Phase 3 Aspirin;Placebos
9 Prospective Randomized Trial Comparing Type of Material in Repair of Congenital Diaphragmatic Hernia Terminated NCT00257946 Phase 3
10 Tracheal Occlusion Guided by Percutaneous Fetoscopy in Fetuses With Severe Isolated Congenital Diaphragmatic Hernia Unknown status NCT01302977 Phase 2
11 "Early" Versus "Standard" Fetal Endoscopic Tracheal Occlusion for Severe Congenital Diaphragmatic Hernia - a Randomized Controlled Trial Unknown status NCT01731509 Phase 2
12 Randomized Clinical Trial in Order to Assess the Effect of Fetoscopic Tracheal Balloon Occlusion on the Postnatal Disease Course in Neonates With Left Congenital Diaphragmatic Hernia - FDH-ECMO/BALLOON-TRIAL Unknown status NCT00373438 Phase 2
13 "Nanotechnologies Applied to General Surgery and Emergency Surgery: The Buckypaper as a New Fixing Method for Prosthetic Materials in the Treatment of Abdominal Wall Hernias, Diaphragmatic Hernias, Diaphragmatic Rupture, Incisional Hernia and Abdominal Wall Disaster in Laparotomy Procedure and Laparoscopic Procedures". Unknown status NCT02137018 Phase 1, Phase 2
14 Milrinone in Congenital Diaphragmatic Hernia Recruiting NCT02951130 Phase 2 Milrinone;Placebo (5% Dextrose)
15 TOTAL TRIAL: Randomized Trial of Fetoscopic Endoluminal Tracheal Occlusion (FETO) Versus Expectant Management During Pregnancy in Fetuses With Left-Sided and Isolated Congenital Diaphragmatic Hernia and Moderate Pulmonary Hypoplasia Active, not recruiting NCT02875860 Phase 2
16 Effect of a Parenteral Emulsion Parenteral With Long-chain Polyunsaturated Fatty Acids Omega 3 on Clinical Outcomes, Inflammatory and Oxidative Stress Markers in Neonates With Persistent Pulmonary Hypertension Not yet recruiting NCT04031508 Phase 2
17 Phase 2 Fetal Tracheal Balloon (IDE G080077) Study in Diaphragmatic Hernia Terminated NCT00966823 Phase 2
18 Safety and Single Dose Population Pharmacokinetics and Bioavailability of Methadone and Its Enantiomers in Newborns and Young Infants At 29-48 Weeks Post Menstrual Age Completed NCT00715988 Phase 1 Methadone HCl Inject 10 mg/ml (will require dilution);Methadone
19 Umbilical Cord Blood Mononuclear Cells for Hypoxic Neurologic Injury in Infants With Congenital Diaphragmatic Hernia (CDH) Recruiting NCT03526588 Phase 1
20 Hypercapnia During Thoracoscopy or Open Surgery for Repair of Oesophageal Atresia With Tracheo-oesophageal Fistula or Congenital Diaphragmatic Hernia in Neonates: Pilot Randomised Controlled Trial Unknown status NCT01467245
21 Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia Unknown status NCT01098929
22 ECMO in Newborn Infants: Circulatory Changes in Relation to Venovenous and Venoarterial Bypass. Implications for Peripheral Organ Circulation Unknown status NCT00622492
23 Pilot Trial of Fetoscopic Endoluminal Tracheal Occlusion (FETO) in Severe Left Congenital Diaphragmatic Hernia (CDH) Completed NCT02596802
24 Investigation of Airway Inflammation in Congenital Diaphragmatic Hernia Patients Completed NCT02453750 Hypersaline;Bronchodilator Response
25 Prospective Data Collection of Patients < 6 Months of Age Undergoing Thoracoscopic Surgery Completed NCT02033772
26 Inflammatory Cytokine Quantification in Infants With Documented Sepsis, Congenital Diaphragmatic Hernia and/or ECMO Therapy Completed NCT01155830
27 Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia Completed NCT02175264
28 Early Childhood Follow-up of Congenital Diaphragmatic Hernia Survivors Completed NCT01029665
29 Observational Longitudinal Study in Children With the Diagnosis of Diaphragmatic Hernia and/or Oesophageal Atresia for Assessing Lung Function Parameters and Quality of Life Completed NCT02466451
30 Molecular Genetic Analysis of Fraser Syndrome and Fryns Syndrome Completed NCT00032877
31 Anesthetic Management in Fetoscopic Surgery and Incidence of Complications - A Retrospective Review Completed NCT02434926
32 Evaluation of New Methods for Prediction of Fetal Lung Maturity in Diabetic Mothers Completed NCT03159234
33 Early Prediction of Cerebral Palsy in Preterm Infants and Term Infants Using Detection of Generalized Movements Completed NCT00749008
34 Estimation of Umbilical Venous Catheter Insertion Depth in Newborns Using Weight or Body Measurement: A Randomized Trial Completed NCT02939690
35 Sustained Inflations to Achieve Lung Aeration at Birth - a Randomized Control Trial Completed NCT01739114
36 Caffeine Citrate for the Treatment of Apnea Associated With Bronchiolitis in Young Infants: A Randomized, Double Blind, Controlled Trial (RCT) Completed NCT01435486 Caffeine citrate;Normal saline
37 Antibody Secreting Cell (ASC) and Immunoactive Protein Profiles in Neonates on Extracorporeal Membrane Oxygenation (ECMO) Completed NCT00371241
38 Integrated Prediction of Extubation Outcome by the Spontaneous Breathing Trial in Newborn Infants Completed NCT03956511
39 Evaluation of the Follow me Mode of the AutoLap System - a Feasibility Study Completed NCT02326870
40 Volumetric Three-dimensional Analysis of the Pediatric Upper Airway Shape Using Computed Tomography Imaging. Completed NCT02771171
41 Intra-Abdominal Hypertension in Neonatal Intensive Care Patients Completed NCT00747552
42 The Biologic Basis of Hernia Formation Completed NCT01099033
43 Randomized Control Trial Evaluating The Effect Of Patterned Oral Somatosensory Entrainment Stimulation Program (NTrainer System) On Suck Development and Feeding Performance of Preterm Infants Born Between 23 And 34 Weeks Gestational Age Completed NCT01069744
44 Diaphragmatic Hernia Research & Exploration, Advancing Molecular Science Recruiting NCT00950118
45 Pilot Trial of Fetoscopic Endoluminal Tracheal Occlusion (FETO) in Severe Left Congenital Diaphragmatic Hernia (CDH) Recruiting NCT02530073
46 Optimisation of Neonatal Ventilation: Congenital Diaphragmatic Hernia - Determining the Appropriate Level of Volume Guarantee Recruiting NCT02849054
47 Feto-Endoscopic Tracheal Occlusion (FETO) for Left Congenital Diaphragmatic Hernia Recruiting NCT02986087
48 Pilot Trial of Fetoscopic Endoluminal Tracheal Occlusion (FETO) in Severe Left Congenital Diaphragmatic Hernia (CDH) Recruiting NCT02549820
49 Physiologic Pilot Study: Work of Breathing Description in Neonates With Congenital Diaphragmatic Hernia in Post-surgical Period Alternatively in Conventional Ventilation (Pressure Controlled) and in NAVA (Neurally Adjusted Ventilatory Assist) Ventilation. Recruiting NCT03250793
50 The Role of 3D Images and Models to Aid Management of Cases of Congenital Diaphragmatic Hernia Diagnosed in the Antenatal Period. Consecutive Patients Studied From Diagnosis to Post Operative Period. Recruiting NCT03750266

Search NIH Clinical Center for Diaphragmatic Hernia, Congenital

Cochrane evidence based reviews: hernia, diaphragmatic

Genetic Tests for Diaphragmatic Hernia, Congenital

Genetic tests related to Diaphragmatic Hernia, Congenital:

# Genetic test Affiliating Genes
1 Congenital Diaphragmatic Hernia 29

Anatomical Context for Diaphragmatic Hernia, Congenital

MalaCards organs/tissues related to Diaphragmatic Hernia, Congenital:

41
Lung, Heart, Fetal Lung, Liver, Kidney, Endothelial, Smooth Muscle

Publications for Diaphragmatic Hernia, Congenital

Articles related to Diaphragmatic Hernia, Congenital:

(show top 50) (show all 4392)
# Title Authors PMID Year
1
Candidate genes for congenital diaphragmatic hernia from animal models: sequencing of FOG2 and PDGFRalpha reveals rare variants in diaphragmatic hernia patients. 38 8 71
17568391 2007
2
The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia. 38 4 8
29618029 2018
3
Prevalence and penetrance of ZFPM2 mutations and deletions causing congenital diaphragmatic hernia. 38 4 71
24702427 2015
4
Genetic aspects of human congenital diaphragmatic hernia. 38 4 8
18510546 2008
5
Infants with Bochdalek diaphragmatic hernia: sibling precurrence and monozygotic twin discordance in a hospital-based malformation surveillance program. 38 4 8
16094667 2005
6
Fog2 is required for normal diaphragm and lung development in mice and humans. 38 4 71
16103912 2005
7
Novel ZFPM2/FOG2 variants in patients with double outlet right ventricle. 38 71
21919901 2012
8
Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia. 38 8
21525063 2011
9
Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH. 38 8
20799323 2010
10
Population-based analysis of left- and right-sided diaphragmatic hernias demonstrates different frequencies of selected additional anomalies. 38 8
18008313 2007
11
Genetic factors in congenital diaphragmatic hernia. 38 8
17436238 2007
12
Array comparative genomic hybridization in patients with congenital diaphragmatic hernia: mapping of four CDH-critical regions and sequencing of candidate genes at 15q26.1-15q26.2. 38 8
16736036 2006
13
Congenital diaphragmatic hernia associated with duplication of 11q23-qter. 38 8
16770801 2006
14
Congenital Diaphragmatic Hernia Overview 38 71
20301533 2006
15
Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): a possible locus for Fryns syndrome. 38 8
16333846 2006
16
Narrowing the candidate region for congenital diaphragmatic hernia in chromosome 15q26: contradictory results. 38 8
16252246 2005
17
Mouse lacking COUP-TFII as an animal model of Bochdalek-type congenital diaphragmatic hernia. 38 8
16251273 2005
18
Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1. 38 8
16141010 2005
19
Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization. 38 8
15750894 2005
20
Congenital diaphragmatic hernia: is 15q26.1-26.2 a candidate locus? 38 8
15057983 2004
21
A genetic model for a central (septum transversum) congenital diaphragmatic hernia in mice lacking Slit3. 38 8
12702769 2003
22
Unilateral agenesis of the diaphragm: a separate entity or an extremely large defect? 38 8
10370024 1999
23
Congenital diaphragmatic hernia with probable autosomal recessive inheritance in an extended consanguineous Pakistani pedigree. 38 8
9222974 1997
24
Congenital diaphragmatic hernia. Epidemiology and outcome. 38 8
8982563 1996
25
Long-term outlook for survivors of congenital diaphragmatic hernia. 38 8
8982576 1996
26
A prospective study of the outcome for fetuses with diaphragmatic hernia. 38 8
8054005 1994
27
Familial congenital diaphragmatic hernia: prenatal diagnosis, management, and outcome. 38 8
8309897 1993
28
Unusual varieties of diaphragmatic herniae. 38 8
1907381 1991
29
Outcomes of Congenital Diaphragmatic Hernia in One of the Twins. 38 4
30609432 2019
30
De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders. 38 4
30532227 2018
31
Prenatal profile of Pallister-Killian syndrome: Retrospective analysis of 114 pregnancies, literature review and approach to prenatal diagnosis. 38 4
30289601 2018
32
Defining outcomes following congenital diaphragmatic hernia using standardised clinical assessment and management plan (SCAMP) methodology within the CDH EURO consortium. 38 4
29915407 2018
33
Prenatal Diagnosis of Congenital Diaphragmatic Hernia: Does Laterality Predict Perinatal Outcomes? 38 4
29304545 2018
34
PBX transcription factors drive pulmonary vascular adaptation to birth. 38 4
29251627 2018
35
Epidemiology and Prognosis of Congenital Diaphragmatic Hernia: A Population-Based Cohort Study in Utah. 38 4
28925604 2017
36
Procedure-Related Complications and Survival Following Fetoscopic Endotracheal Occlusion (FETO) for Severe Congenital Diaphragmatic Hernia: Systematic Review and Meta-Analysis in the FETO Era. 38 4
27522127 2017
37
Congenital diaphragmatic hernia-associated pulmonary hypertension. 38 4
28641752 2017
38
ECMO in CDH: Is there a role? 38 4
28641755 2017
39
Genome-wide enrichment of damaging de novo variants in patients with isolated and complex congenital diaphragmatic hernia. 38 4
28303347 2017
40
Whole-Exome Sequencing in Nine Monozygotic Discordant Twins. 38 4
26681452 2016
41
Standardized Postnatal Management of Infants with Congenital Diaphragmatic Hernia in Europe: The CDH EURO Consortium Consensus - 2015 Update. 38 4
27077664 2016
42
Clinical characteristics and outcomes of patients with right congenital diaphragmatic hernia: A population-based study. 38 4
25783377 2015
43
ASSOCIATED NON DIAPHRAGMATIC ANOMALIES AMONG CASES WITH CONGENITAL DIAPHRAGMATIC HERNIA. 38 4
26625659 2015
44
Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia. 38 4
23138528 2013
45
Premature differentiation of vascular smooth muscle cells in human congenital diaphragmatic hernia. 38 4
23018129 2013
46
Sensorineural hearing loss and language development following neonatal extracorporeal membrane oxygenation. 38 4
23249782 2013
47
Prediction of chronic lung disease, survival and need for ECMO therapy in infants with congenital diaphragmatic hernia: additional value of fetal MRI measurements? 38 4
21458944 2012
48
Copy number detection in discordant monozygotic twins of Congenital Diaphragmatic Hernia (CDH) and Esophageal Atresia (EA) cohorts. 38 4
22071887 2012
49
The correlation between lung volume and liver herniation measurements by fetal MRI in isolated congenital diaphragmatic hernia: a systematic review and meta-analysis of observational studies. 38 4
21915885 2011
50
New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle. 71
20807224 2011

Variations for Diaphragmatic Hernia, Congenital

ClinVar genetic disease variations for Diaphragmatic Hernia, Congenital:

6 (show all 24)
# Gene Variation Type Significance SNP ID GRCh37 Pos GRCh38 Pos
1 GATA6 NM_005257.5(GATA6): c.712G> T (p.Gly238Ter) single nucleotide variant Pathogenic rs587777710 18:19751817-19751817 18:22171856-22171856
2 GATA6 NM_005257.5(GATA6): c.1072del (p.Val358fs) deletion Pathogenic rs1555628863 18:19752177-19752177 18:22172216-22172216
3 GATA6 NM_005257.5(GATA6): c.1366C> T (p.Arg456Cys) single nucleotide variant Pathogenic rs387906818 18:19761477-19761477 18:22181516-22181516
4 46;XX;t(7;13)(p13;q34)dn Translocation Pathogenic
5 PGAP3 NM_033419.5(PGAP3): c.851A> G (p.His284Arg) single nucleotide variant Pathogenic 17:37829352-37829352 17:39673099-39673099
6 CDK8 NM_001260.3(CDK8): c.185C> A (p.Ser62Ter) single nucleotide variant Pathogenic 13:26911760-26911760 13:26337623-26337623
7 FBN1 NM_000138.4(FBN1): c.4970_4971insA (p.Cys1658fs) insertion Likely pathogenic rs864309713 15:48756190-48756191 15:48463993-48463994
8 FRAS1 NM_025074.7(FRAS1): c.2389G> A (p.Glu797Lys) single nucleotide variant risk factor rs372359356 4:79258938-79258938 4:78337784-78337784
9 FRAS1 NM_025074.7(FRAS1): c.6323A> T (p.Asp2108Val) single nucleotide variant risk factor rs921444831 4:79371353-79371353 4:78450199-78450199
10 GLI3 NM_000168.6(GLI3): c.2726C> G (p.Ala909Gly) single nucleotide variant risk factor rs780263938 7:42005945-42005945 7:41966347-41966347
11 ROBO4 NM_019055.6(ROBO4): c.569G> C (p.Gly190Ala) single nucleotide variant risk factor rs756636036 11:124766204-124766204 11:124896308-124896308
12 FREM2 NM_207361.6(FREM2): c.4994C> T (p.Ser1665Phe) single nucleotide variant risk factor rs1555261576 13:39266475-39266475 13:38692338-38692338
13 FREM2 NM_207361.6(FREM2): c.5940_5942del (p.Leu1981del) deletion Likely pathogenic rs775394591 13:39358864-39358866 13:38784727-38784729
14 NIPBL NM_015384.5(NIPBL): c.1811_1812del (p.Lys603_Ser604insTer) deletion Likely pathogenic rs1057518944 5:36985092-36985093 5:36984990-36984991
15 MYO15A NM_016239.4(MYO15A): c.1454T> C (p.Val485Ala) single nucleotide variant Conflicting interpretations of pathogenicity rs200532919 17:18023568-18023568 17:18120254-18120254
16 FRAS1 NM_025074.7(FRAS1): c.9806G> A (p.Arg3269Gln) single nucleotide variant Conflicting interpretations of pathogenicity rs61729366 4:79432453-79432453 4:78511299-78511299
17 PAX3 NM_181457.4(PAX3): c.944C> A (p.Thr315Lys) single nucleotide variant Conflicting interpretations of pathogenicity rs2234675 2:223085955-223085955 2:222221236-222221236
18 FREM1 NM_144966.5(FREM1): c.1394G> C (p.Gly465Ala) single nucleotide variant Conflicting interpretations of pathogenicity rs41298151 9:14842658-14842658 9:14842660-14842660
19 MET NM_001127500.3(MET): c.3029C> T (p.Thr1010Ile) single nucleotide variant Conflicting interpretations of pathogenicity rs56391007 7:116411990-116411990 7:116771936-116771936
20 DES NM_001927.4(DES): c.638C> T (p.Ala213Val) single nucleotide variant Conflicting interpretations of pathogenicity rs41272699 2:220284876-220284876 2:219420154-219420154
21 46;X;t(X;10)(p11.2;q24.3) Translocation Uncertain significance
22 DEPDC5 NM_001242897.2(DEPDC5): c.2551G> A (p.Gly851Ser) single nucleotide variant Uncertain significance 22:32239782-32239782 22:31843796-31843796
23 46;XY;t(1;6)(p22;q15)dn Translocation Uncertain significance
24 FREM2 NM_207361.6(FREM2): c.4031G> A (p.Arg1344His) single nucleotide variant Uncertain significance rs143044921 13:39265512-39265512 13:38691375-38691375

Copy number variations for Diaphragmatic Hernia, Congenital from CNVD:

7 (show top 50) (show all 94)
# CNVD ID Chromosom Start End Type Gene Symbol CNVD Disease
1 15857 1 119957963 119994447 Deletion HSD3B2 Congenital diaphragmatic hernia
2 23597 1 171936289 171970634 In DNM3 Congenital diaphragmatic hernia
3 27740 1 212100000 222100000 Deletion DISP1 Congenital diaphragmatic hernia
4 27744 1 212100000 222100000 Deletion HLX Congenital diaphragmatic hernia
5 27754 1 212100000 225100000 Deletion Congenital diaphragmatic hernia
6 28522 1 223073839 225318623 Deletion C1orf65 Congenital diaphragmatic hernia
7 28523 1 223073839 225318623 Deletion CAPN2 Congenital diaphragmatic hernia
8 28524 1 223073839 225318623 Deletion CAPN8 Congenital diaphragmatic hernia
9 28525 1 223073839 225318623 Deletion DEGS1 Congenital diaphragmatic hernia
10 28526 1 223073839 225318623 Deletion DISP1 Congenital diaphragmatic hernia
11 28527 1 223073839 225318623 Deletion DNAH14 Congenital diaphragmatic hernia
12 28528 1 223073839 225318623 Deletion FBXO28 Congenital diaphragmatic hernia
13 28529 1 223073839 225318623 Deletion MIR320B2 Congenital diaphragmatic hernia
14 28530 1 223073839 225318623 Deletion NVL Congenital diaphragmatic hernia
15 28531 1 223073839 225318623 Deletion SUSD4 Congenital diaphragmatic hernia
16 28532 1 223073839 225318623 Deletion TLR5 Congenital diaphragmatic hernia
17 28533 1 223073839 225318623 Deletion TP53BP2 Congenital diaphragmatic hernia
18 28534 1 223073839 225318623 Deletion WDR26 Congenital diaphragmatic hernia
19 35588 1 65137345 65218480 In CACHD1 Congenital diaphragmatic hernia
20 35589 1 65137345 65218480 In RAVER2 Congenital diaphragmatic hernia
21 49978 11 112347267 134927114 Der Congenital diaphragmatic hernia
22 52746 11 19168012 32271202 Der Congenital diaphragmatic hernia
23 59704 11 77270540 77431584 In AQP11 Congenital diaphragmatic hernia
24 59705 11 77270540 77431584 In CLNS1A Congenital diaphragmatic hernia
25 59706 11 77270540 77431584 In RSF1 Congenital diaphragmatic hernia
26 64289 12 12600000 14800000 Deletion RAIG1 Congenital diaphragmatic hernia
27 69076 12 5300000 10000000 Deletion RBP5 Congenital diaphragmatic hernia
28 79371 13 70666491 71594524 In ATXN8OS Congenital diaphragmatic hernia
29 79372 13 70666491 71594524 In KLHL1 Congenital diaphragmatic hernia
30 79373 13 70666491 71594524 In SCA8 Congenital diaphragmatic hernia
31 85160 14 39875206 40301762 Deletion FBXO33 Congenital diaphragmatic hernia
32 93300 15 50791758 50833347 Deletion USP50 Congenital diaphragmatic hernia
33 93301 15 50791758 50833347 Deletion USP8 Congenital diaphragmatic hernia
34 93579 15 55800000 65300000 Deletion Congenital diaphragmatic hernia
35 94339 15 65300000 76100000 Deletion Congenital diaphragmatic hernia
36 94505 15 67540042 68049656 Deletion AAGAB Congenital diaphragmatic hernia
37 94506 15 67540042 68049656 Deletion C15orf61 Congenital diaphragmatic hernia
38 94507 15 67540042 68049656 Deletion IQCH Congenital diaphragmatic hernia
39 94508 15 67540042 68049656 Deletion MAP2K5 Congenital diaphragmatic hernia
40 95359 15 75600108 75648132 In COMMD4 Congenital diaphragmatic hernia
41 95360 15 75600108 75648132 In NEIL1 Congenital diaphragmatic hernia
42 95413 15 76100000 79500000 Deletion CRABP1 Congenital diaphragmatic hernia
43 95695 15 79500000 83000000 Deletion Congenital diaphragmatic hernia
44 95710 15 79500000 83000000 Microdeletions AP3B2 Congenital diaphragmatic hernia
45 95711 15 79500000 83000000 Microdeletions CPEB1 Congenital diaphragmatic hernia
46 95712 15 79500000 83000000 Microdeletions HDGFRP3 Congenital diaphragmatic hernia
47 95713 15 79500000 83000000 Microdeletions HOMER2 Congenital diaphragmatic hernia
48 96233 15 86900000 96300000 Deletion Congenital diaphragmatic hernia
49 96719 15 92100000 96300000 Deletion Congenital diaphragmatic hernia
50 97350 16 1 6300000 Gain Congenital diaphragmatic hernia

Expression for Diaphragmatic Hernia, Congenital

Search GEO for disease gene expression data for Diaphragmatic Hernia, Congenital.

Pathways for Diaphragmatic Hernia, Congenital

Pathways related to Diaphragmatic Hernia, Congenital according to GeneCards Suite gene sharing:

# Super pathways Score Top Affiliating Genes
1
Show member pathways
12.04 PAX3 NKX2-1 GATA6 GATA4
2 11.62 WT1 GATA4 FGF10
3 11.08 PAX3 NR2F2 GLI3 GATA6
4 10.79 GATA6 GATA4 FGF10
5 10.11 NKX2-1 GLI3

GO Terms for Diaphragmatic Hernia, Congenital

Cellular components related to Diaphragmatic Hernia, Congenital according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 basement membrane GO:0005604 8.8 FREM2 FREM1 FRAS1

Biological processes related to Diaphragmatic Hernia, Congenital according to GeneCards Suite gene sharing:

(show all 44)
# Name GO ID Score Top Affiliating Genes
1 in utero embryonic development GO:0001701 9.92 ZFPM2 NR2F2 GLI3 GATA6
2 kidney development GO:0001822 9.85 WT1 STRA6 GLI3
3 male gonad development GO:0008584 9.84 WT1 GATA6 GATA4
4 epithelial cell differentiation GO:0030855 9.83 WT1 GATA6 FGF10
5 lung development GO:0030324 9.83 ZFPM2 STRA6 NKX2-1 GLI3 FGF10
6 forebrain development GO:0030900 9.82 NR2F2 NKX2-1 GLI3
7 camera-type eye development GO:0043010 9.81 WT1 STRA6 GLI3
8 cell communication GO:0007154 9.76 FREM2 FREM1 FRAS1
9 limb development GO:0060173 9.72 NR2F2 GLI3 FGF10
10 thyroid gland development GO:0030878 9.69 NKX2-1 FGF10
11 cardiac muscle cell differentiation GO:0055007 9.69 GATA6 GATA4
12 limb morphogenesis GO:0035108 9.69 GLI3 FGF10
13 adrenal gland development GO:0030325 9.68 WT1 STRA6
14 morphogenesis of an epithelium GO:0002009 9.68 FREM2 FRAS1
15 aortic valve morphogenesis GO:0003180 9.68 GATA4 ELN
16 embryonic digestive tract morphogenesis GO:0048557 9.67 GLI3 FGF10
17 cardiac muscle tissue development GO:0048738 9.67 ZFPM2 GATA6
18 epithelial tube branching involved in lung morphogenesis GO:0060441 9.67 NKX2-1 FGF10
19 smooth muscle cell differentiation GO:0051145 9.66 GATA6 FGF10
20 diaphragm development GO:0060539 9.65 WT1 STRA6
21 positive regulation of male gonad development GO:2000020 9.63 ZFPM2 WT1
22 cellular response to gonadotropin stimulus GO:0071371 9.63 WT1 GATA6
23 embryonic digestive tract development GO:0048566 9.63 STRA6 GLI3 FGF10
24 intestinal epithelial cell differentiation GO:0060575 9.62 GATA6 GATA4
25 forebrain dorsal/ventral pattern formation GO:0021798 9.61 NKX2-1 GLI3
26 positive regulation of transcription, DNA-templated GO:0045893 9.61 ZFPM2 WT1 PAX3 NR2F2 NKX2-1 GLI3
27 positive regulation of cardioblast differentiation GO:0051891 9.6 GATA6 GATA4
28 animal organ formation GO:0048645 9.59 GATA6 FGF10
29 transcription by RNA polymerase II GO:0006366 9.58 PAX3 GATA6
30 type II pneumocyte differentiation GO:0060510 9.58 NKX2-1 GATA6 FGF10
31 metanephros morphogenesis GO:0003338 9.57 FRAS1 FGF10
32 Clara cell differentiation GO:0060486 9.56 NKX2-1 GATA6
33 heart development GO:0007507 9.55 ZFPM2 WT1 STRA6 GLI3 FREM2
34 lung saccule development GO:0060430 9.54 NKX2-1 GATA6 FGF10
35 nose morphogenesis GO:0043585 9.52 STRA6 GLI3
36 negative regulation of female gonad development GO:2000195 9.51 ZFPM2 WT1
37 mammary gland specification GO:0060594 9.49 GLI3 FGF10
38 anatomical structure formation involved in morphogenesis GO:0048646 9.26 NKX2-1 GLI3
39 tissue development GO:0009888 9.18 WT1
40 animal organ morphogenesis GO:0009887 8.92 PAX3 NKX2-1 FGF10 ELN
41 regulation of transcription, DNA-templated GO:0006355 10.21 WT1 TEF PAX3 NR2F2 NKX2-1 GLI3
42 negative regulation of transcription by RNA polymerase II GO:0000122 10.13 ZFPM2 WT1 NR2F2 NKX2-1 GLI3 GATA6
43 positive regulation of transcription by RNA polymerase II GO:0045944 10.02 ZFPM2 WT1 TEF PAX3 NKX2-1 GLI3
44 negative regulation of transcription, DNA-templated GO:0045892 10.01 ZFPM2 WT1 NR2F2 NKX2-1 GLI3 GATA6

Molecular functions related to Diaphragmatic Hernia, Congenital according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 DNA binding GO:0003677 9.91 ZFPM2 WT1 TEF PAX3 NR2F2 NKX2-1
2 DNA-binding transcription factor activity, RNA polymerase II-specific GO:0000981 9.81 ZFPM2 WT1 TEF PAX3 NR2F2 NKX2-1
3 RNA polymerase II regulatory region sequence-specific DNA binding GO:0000977 9.67 TEF NKX2-1 GLI3 GATA4
4 transcription regulatory region DNA binding GO:0044212 9.62 WT1 NKX2-1 GATA6 GATA4
5 DNA-binding transcription factor activity GO:0003700 9.56 WT1 TEF PAX3 NR2F2 NKX2-1 GLI3
6 sequence-specific DNA binding GO:0043565 9.23 WT1 TEF PAX3 NR2F2 NKX2-1 GLI3
7 enhancer sequence-specific DNA binding GO:0001158 9.1 GATA4

Sources for Diaphragmatic Hernia, Congenital

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 TGDB
71 Tocris
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73 UMLS via Orphanet
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