Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Sacral spina bifida with hydrocephalus - closed (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Fissured spine with hydrocephalus |
Associated morphology |
False |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Lumbar spina bifida with hydrocephalus - open |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Lumbar spina bifida with hydrocephalus |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Acquired dilation of bile duct |
Associated morphology |
False |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hydrocephalus with endocardial fibroelastosis and cataract syndrome (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hirschsprung disease-nail hypoplasia-dysmorphism syndrome is a fatal malformative disorder that is characterised by Hirschsprung disease, hypoplastic nails, distal limb hypoplasia and minor craniofacial dysmorphic features (flat facies, upward slanting palpebral fissures, narrow philtrum, narrow, high arched palate, micrognathia, low set ears with abnormal helices). Hydronephrosis has also been reported. There have been no further descriptions in the literature since 1988. |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Acquired hydrocephalus of newborn |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hydrocephalus, cardiac malformation, dense bone syndrome (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Congenital dilation of right pulmonary artery (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of cardiac ventricle |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Waardenburg-Shah syndrome (WSS), also known as Waardenburg syndrome type 4 (WS4) is characterized by the association of Waardenburg syndrome (sensorineural hearing loss and pigmentary abnormalities) and Hirschsprung disease (aganglionic megacolon). |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilation of left pulmonary artery (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of pulmonary artery (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
L1 syndrome |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of ductus arteriosus |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Secondary megacolon - congenital |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hydrocephalus, tall stature, joint laxity syndrome (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Congenital dilatation of atrium |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Growth delay - hydrocephaly - lung hypoplasia, also named Game-Friedman-Paradice syndrome, is a rare developmental disorder described in 4 siblings so far and characterised by delayed fetal growth, hydrocephaly with patent aqueduct of Sylvius, underdeveloped lungs and various other anomalies such as small jaw, intestinal malrotation, omphalocele, shortness of lower limbs, bowed tibias and foot deformities. |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Extensive aganglionosis Hirschsprung disease (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Congenital cystic bronchiectasis |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Total intestinal aganglionosis (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilation of ascending aorta (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Capra DeMarco syndrome |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Congenital primary megaureter (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Giant esophagus |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Short segment Hirschsprung's disease |
Associated morphology |
False |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Congenital enlargement of coronary sinus |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of trachea (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Haddad syndrome (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
A rare multiple congenital anomalies characterized by the association of Vertebral anomalies, Anal atresia, Congenital cardiac disease, Tracheoesophageal fistula, Renal anomalies, and Limb defects (acronym VACTERL) with hydrocephalus. Association with hydrocephalus is relatively rare, may be distinct from VACTERL association in general, and may follow an autosomal recessive pattern of inheritance in some individuals. |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of aorta |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilation of bile duct |
Associated morphology |
False |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Caroli disease |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of lobar intrahepatic bile duct (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Mowat-Wilson syndrome (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Agenesis of cerebellum and hydrocephalus syndrome (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of stomach |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
A rare multiple congenital anomalies syndrome characterised principally by Sprengel anomaly (upward displacement of the scapula) and hydrocephaly. Other anomalies such as global developmental delay, psychosis, brachydactyly, and costovertebral dysplasia may also be present. |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Congenital dilatation of inferior vena cava |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hirschsprung disease with deafness and polydactyly syndrome |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Congenital dilatation of innominate artery |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of bladder |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of colon (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hydrocephalus, blue sclera, nephropathy syndrome (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Bilateral congenital primary hydronephrosis (disorder) |
Associated morphology |
False |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Aganglionosis of Auerbach's plexus (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Congenital bronchiectasis |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital megaduodenum (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital hydrocephalus caused by toxoplasmosis |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of renal pelvis (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital obstructive hydrocephalus (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
syndrome d'Okamoto |
Associated morphology |
False |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ectasia of left atrial appendage |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of subclavian artery |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hirschsprung disease with type D brachydactyly syndrome |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Familial idiopathic dilatation of right atrium |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Megacystis-megaureter syndrome (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital aganglionic megacolon (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital hydrocephalus |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hydrocephalus with obesity and hypogonadism syndrome |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
macrocolôn congénital non aganglionique |
Associated morphology |
False |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ectasia of right atrial appendage (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of superior vena cava |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of intestinal tract |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of carotid artery |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Familial thoracic aortic aneurysm and aortic dissection |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of esophagus |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of aortic arch (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of ureter (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital dilatation of aortic root (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hirschsprung disease of rectosigmoid region |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Megalourethra |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Goldberg Shprintzen megacolon syndrome (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Long segment Hirschsprung's disease (disorder) |
Associated morphology |
False |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Fetal hydrocephalus (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hirschsprung disease, ganglioneuroblastoma syndrome |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Myelocele with hydrocephalus |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Corneal ectasia |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pellucid marginal degeneration of cornea of bilateral eyes (disorder) |
Associated morphology |
False |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Pellucid marginal degeneration of cornea of left eye |
Associated morphology |
False |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Pellucid marginal degeneration of cornea of right eye (disorder) |
Associated morphology |
False |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Corneal ectasia of bilateral eyes (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Corneal ectasia of bilateral eyes (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Corneal ectasia of right eye |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acquired keratoglobus |
Associated morphology |
False |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Pellucid marginal corneal degeneration (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Corneal ectasia of left eye |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Descemetocele (disorder) |
Associated morphology |
False |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Thoracic dysplasia and hydrocephalus syndrome (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Corneal ectasia due to and following laser in situ keratomileusis (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hydrocalycosis |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hydromyelocele with hydrocephalus |
Associated morphology |
False |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Congenital keratoglobus |
Associated morphology |
False |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Port-wine nevi, mega cisterna magna, hydrocephalus syndrome |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acquired dilation of bile duct |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Mammary duct ectasia of right breast (disorder) |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Mammary duct ectasia of left breast |
Associated morphology |
True |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acquired keratoglobus |
Associated morphology |
False |
Dilatation |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |