| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Didymosis aplasticosebacea (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Encephalocraniocutaneous lipomatosis |
est un(e) (attribut) |
False |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| syndrome de microdélétion 14q22q23 |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Ocular motor apraxia Cogan type (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Encephalocele of orbit |
est un(e) (attribut) |
False |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Alstrom syndrome |
est un(e) (attribut) |
False |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Aicardi's syndrome |
est un(e) (attribut) |
False |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Congenital blindness |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Congenital anomaly of eye |
est un(e) (attribut) |
False |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Cerebrofacial arteriovenous metameric syndrome type 2 |
est un(e) (attribut) |
False |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Cilioretinal artery (finding) |
est un(e) (attribut) |
False |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Congenital anomaly of optic nerve |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Congenital strabismus |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts |
est un(e) (attribut) |
False |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Congenital anomaly of ocular adnexa |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Congenital anomaly of eye |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Congenital anomaly of orbit proper (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Congenital vascular anomaly of eye |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Congenital malformation of eye, ear and neck |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Heide syndrome |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Karsch Neugebauer syndrome |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Oculogastrointestinal muscular dystrophy (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Macrocephaly, obesity, mental disability, ocular abnormality syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Congenital absence of optic chiasma (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Congenital malformation of the eyebrow |
est un(e) (attribut) |
False |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|
| Autosomal recessive chorioretinopathy and microcephaly syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital anomaly of visual system |
Inferred relationship |
Some |
|