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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Abnormalities, Drug-Induced +   
Abnormalities, Severe Teratoid +   
Absence of Nasal Bones 
Absence of Vagina 
Accessory Pancreas 
Agenesis of Gallbladder  
agnathia-otocephaly complex  
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency  
Aicardi syndrome  
Amastia +   
Arrhinia 
arthrogryposis multiplex congenita +   
Atlanto-Axial Fusion 
autosomal dominant congenital deafness with onychodystrophy  
autosomal recessive congenital ichthyosis +   
bladder exstrophy-epispadias-cloacal exstrophy complex +   
blepharophimosis +   
Bresheck/Bresek Syndrome 
Cardiovascular Abnormalities +   
Caudal Duplication Anomaly  
caudal regression syndrome  
chromosomal disease +   
cleft palate-lateral synechia syndrome  
Complete Absence of Bile and Pancreatic Ducts 
Complete Agenesis of Diaphragm 
Compton-North congenital myopathy  
congenital adrenal hyperplasia +   
congenital adrenal insufficiency  
congenital afibrinogenemia +   
congenital amegakaryocytic thrombocytopenia +   
congenital aphakia  
Congenital Aural Atresia  
congenital bilateral absence of vas deferens +   
congenital bile acid synthesis defect +   
congenital central hypoventilation syndrome +   
congenital chylothorax  
congenital contractural arachnodactyly  
congenital diaphragmatic hernia +   
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. (DO)
congenital diarrhea +   
congenital disorder of glycosylation +   
congenital epulis 
congenital fibrosarcoma  
congenital fibrosis of the extraocular muscles +   
Congenital Foot Deformities +   
congenital generalized lipodystrophy +   
congenital granular cell tumor 
congenital heart block +   
congenital heart disease +   
congenital hemolytic anemia +   
congenital hereditary endothelial dystrophy of cornea  
congenital hypogammaglobulinemia 
congenital hypoplastic anemia +   
congenital hypothyroidism +   
congenital hypotrichosis with juvenile macular dystrophy  
congenital intrinsic factor deficiency  
congenital lactase deficiency  
congenital leptin deficiency  
congenital megabladder  
congenital mesoblastic nephroma +   
Congenital Microtia +   
congenital mirror movement disorder +   
congenital muscular dystrophy +   
congenital myasthenic syndrome +   
congenital myopathy 4A +   
congenital nervous system abnormality +   
congenital nystagmus +   
congenital ptosis +   
congenital stationary night blindness +   
Congenital Stridor 
congenital stromal corneal dystrophy  
congenital structural myopathy +   
congenital sucrase-isomaltase deficiency  
congenital syphilis +  
congenital toxoplasmosis  
Crane-Heise Syndrome 
cryptophthalmia +   
Deal Barratt Dillon Syndrome 
Diaphragmatic Hernia, Traumatic 
Digestive System Abnormalities +   
epidermolysis bullosa with congenital localized absence of skin and deformity of nails  
Eye Abnormalities +   
Familial Cryptotia 
Familial Laryngeal Web 
Fryns Syndrome  
gastroschisis +   
hiatus hernia +   
Hydrocephalus, Skeletal Anomalies, and Mental Disturbance 
hypospadias +   
imperforate anus +   
Klippel-Feil syndrome +   
large congenital melanocytic nevus  
Laryngeal Cleft 
laryngomalacia +   
Leber congenital amaurosis +   
lethal congenital contracture syndrome +   
lethal congenital glycogen storage disease of heart  
Lymphatic Abnormalities +   
Mayer-Rokitansky-Kuster-Hauser syndrome +   
Meckel's diverticulum 
MLS syndrome +   
Mondini Dysplasia  
Multiple Abnormalities +   
multiple congenital anomalies-hypotonia-seizures syndrome +   
Musculoskeletal Abnormalities +   
myotonia congenita +   
Nervous System Malformations +   
neural tube defect +   
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES  
non-congenital cyst of kidney 
nonsyndromic congenital nail disorder +   
omphalocele  
orofacial cleft +   
palmoplantar keratoderma and congenital alopecia 1  
palmoplantar keratoderma and congenital alopecia 2 
Pancreas Agenesis, Dorsal 
Poland syndrome 
polydactyly +   
Posterior Lumbosacral Vertebral Fusion with Blepharoptosis 
primary congenital glaucoma +   
Radiation-Induced Abnormalities 
radioulnar synostosis +   
rapidly involuting congenital hemangioma 
Renal and Mullerian Duct Hypoplasia +   
Respiratory System Abnormalities +   
Rhiny 
Saito Kuba Tsuruta Syndrome 
Schlegelberger Grote Syndrome 
severe congenital encephalopathy due to MECP2 mutation  
severe congenital neutropenia +   
Silver-Russell syndrome +   
situs inversus +   
Skin Abnormalities +   
spondylocostal dysostosis 1  
spondyloepiphyseal dysplasia with congenital joint dislocations  
Sprengel Deformity  
Stomatognathic System Abnormalities +   
T-cell immunodeficiency, congenital alopecia, and nail dystrophy  
thyroid malformation +   
TORCH syndrome 
Urogenital Abnormalities +   
visceral heterotaxy +   
Zaki syndrome  
Zika virus congenital syndrome 

Synonyms
Exact Synonyms: Bochdalek hernias ;   CDH ;   DIH ;   HCD ;   Morgagni hernias ;   Morgagni's hernias ;   Morgagnis hernias ;   agenesis of hemidiaphragm ;   congenital diaphragmatic defect ;   congenital diaphragmatic defects
Narrow Synonyms: DIH1 ;   complete agenesis of diaphragm ;   hemidiaphragm, agenesis of diaphragmatic hernia 1
Primary IDs: MESH:D065630
Alternate IDs: MIM:142340
Xrefs: EFO:0007216 ;   GARD:1481 ;   ICD10CM:Q79.0 ;   MIM:PS142340 ;   NCI:C34687 ;   NCI:C98893 ;   ORDO:2140
Definition Sources: http://en.wikipedia.org/wiki/Congenital_diaphragmatic_hernia "DO" "DO", http://ghr.nlm.nih.gov/condition/congenital-diaphragmatic-hernia "DO" "DO"

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