Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Cataract-glaucoma syndrome is characterized by the association of total bilateral congenital cataract with the secondary occurrence of glaucoma appearing at ages varying between 10 and 40 years. |
Is a |
False |
Bilateral cataracts |
Inferred relationship |
Some |
|
Presenile cataract of bilateral eyes (disorder) |
Is a |
True |
Bilateral cataracts |
Inferred relationship |
Some |
|
Cataract of posterior subcapsule of bilateral eyes (disorder) |
Is a |
True |
Bilateral cataracts |
Inferred relationship |
Some |
|
Bilateral posterior capsule opacification (disorder) |
Is a |
True |
Bilateral cataracts |
Inferred relationship |
Some |
|
Diabetic cataract of bilateral eyes |
Is a |
True |
Bilateral cataracts |
Inferred relationship |
Some |
|
Cortical age-related cataract of bilateral eyes (disorder) |
Is a |
True |
Bilateral cataracts |
Inferred relationship |
Some |
|
Congenital cataract of bilateral eyes (disorder) |
Is a |
True |
Bilateral cataracts |
Inferred relationship |
Some |
|
Bilateral eye brunescent cataract |
Is a |
True |
Bilateral cataracts |
Inferred relationship |
Some |
|
Anterior subcapsular polar senile cataract of bilateral eyes (disorder) |
Is a |
False |
Bilateral cataracts |
Inferred relationship |
Some |
|
Hypermature senile cataract of bilateral eyes (disorder) |
Is a |
True |
Bilateral cataracts |
Inferred relationship |
Some |
|
Senile combined form cataract of bilateral eyes (disorder) |
Is a |
True |
Bilateral cataracts |
Inferred relationship |
Some |
|
Bilateral anterior subcapsular polar cataract |
Is a |
True |
Bilateral cataracts |
Inferred relationship |
Some |
|
Bilateral cataract of eyes caused by drug |
Is a |
True |
Bilateral cataracts |
Inferred relationship |
Some |
|
Bilateral cataract of eyes due to and following trauma |
Is a |
True |
Bilateral cataracts |
Inferred relationship |
Some |
|
A rare pervasive developmental disorder characterized by microcephaly, profound developmental delay, intellectual disability, bilateral cataracts, severe epilepsy including infantile spasms, hypotonia, irritability, feeding difficulties leading to failure to thrive, and stereotypic hand movements. The disease manifests in infancy. Brain imaging reveals delay in myelination and cerebral atrophy. |
Is a |
True |
Bilateral cataracts |
Inferred relationship |
Some |
|
Cataract due to and following ocular disease of bilateral eyes (disorder) |
Is a |
True |
Bilateral cataracts |
Inferred relationship |
Some |
|
Bilateral calcified cataracts |
Is a |
True |
Bilateral cataracts |
Inferred relationship |
Some |
|
A rare disorder of fatty acid biosynthesis characterised by spastic paraparesis, bilateral congenital/juvenile cataracts, gross motor developmental delay, speech delay and truncal hypotonia. Seizures in infancy can also be observed. Patients have elevated levels of ether lipids including plasmalogen. Majority of the affected individuals have normal brain imaging and normal growth. No microcephaly or dysmorphic features were reported. |
Is a |
True |
Bilateral cataracts |
Inferred relationship |
Some |
|