Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Dandy-Walker syndrome (disorder) |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Arnold-Chiari syndrome |
Is a |
False |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital stenosis of aqueduct of Sylvius |
Is a |
False |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Spina bifida with hydrocephalus |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Foramen of Magendie atresia (disorder) |
Is a |
False |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Foramen of Luschka atresia (disorder) |
Is a |
False |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital hydrocephalus caused by toxoplasmosis |
Is a |
False |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Other specified congenital hydrocephalus |
Is a |
False |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital hydrocephalus NOS |
Is a |
False |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
[X]Other congenital hydrocephalus |
Is a |
False |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Myelocele with hydrocephalus |
Is a |
False |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Spina bifida with hydrocephalus of late onset |
Is a |
False |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Rachischisis with hydrocephalus |
Is a |
False |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hydromyelocele with hydrocephalus |
Is a |
False |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fetal hydrocephalus suspected (situation) |
Associated finding |
False |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cerebral degeneration due to congenital hydrocephalus |
Due to |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Fetal hydrocephalus suspected (situation) |
Associated finding |
False |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Family history of congenital hydrocephalus |
Associated finding |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Agenesis of cerebellum and hydrocephalus syndrome (disorder) |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
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. |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
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. |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Capra DeMarco syndrome |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hydrocephalus with endocardial fibroelastosis and cataract syndrome (disorder) |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hydrocephalus, cardiac malformation, dense bone syndrome (disorder) |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
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. |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hydrocephalus with obesity and hypogonadism syndrome |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome (disorder) |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hydrocephalus, tall stature, joint laxity syndrome (disorder) |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital obstructive hydrocephalus (disorder) |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hydrocephalus, blue sclera, nephropathy syndrome (disorder) |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
L1 syndrome |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hydrocephalus associated with congenital aqueduct stenosis (disorder) |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Thoracic dysplasia and hydrocephalus syndrome (disorder) |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fetal hydrocephalus (disorder) |
Is a |
False |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Port-wine nevi, mega cisterna magna, hydrocephalus syndrome |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare multiple congenital anomalies/dysmorphic syndrome characterised by congenital hydrocephalus involving the lateral ventricles, low-set umbilicus, bilateral inguinal hernia, and mild facial dysmorphism (such as epicanthal folds, broad, flat nasal bridge, and small, bulbous nose). Additional reported manifestations include unilateral cryptorchidism, vesicoureteral reflux, and tetralogy of Fallot. There have been no further descriptions in the literature since 1993. |
Is a |
True |
Congenital hydrocephalus |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|