Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Optic nerve hypoplasia due to endocrine deficiency |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Optic atrophy due to late congenital syphilis |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Chronic relapsing inflammatory optic neuropathy |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Ocular anomalies, axonal neuropathy, developmental delay syndrome |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
2 |
X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
5 |
Disorder of optic nerve due to micronutrient deficiency |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Disorder of optic nerve due to thiamine deficiency |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Autosomal recessive spastic paraplegia type 74 |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
2 |
X-linked spastic paraplegia type 2 |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal recessive spastic paraplegia type 55 |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
2 |
Autosomal recessive spastic paraplegia type 57 |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
2 |
Spastic paraplegia, optic atrophy, neuropathy syndrome |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
2 |
Multiple mitochondrial dysfunctions syndrome type 4 |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
5 |
Posterior ischemic optic neuropathy due to arteritis |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Phospholipase A2 activating protein-associated neurodevelopmental disorder |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
3 |
Auditory neuropathy, optic atrophy syndrome |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Primary malignant ependymoma of optic nerve |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Primary malignant ependymoma of optic nerve |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
2 |
Idiopathic optic neuritis |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Non-arteritic posterior ischemic optic neuropathy |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Optic neuritis due to demyelinating disease of central nervous system |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Disorder of optic nerve following administration of vaccine to produce active immunity |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
2 |
X-linked optic atrophy |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Primary malignant astrocytoma of optic nerve |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Optic neuritis NOS |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Unspecified optic neuritis |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Unspecified optic atrophy |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Optic atrophy NOS |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |
Hereditary optic atrophy NOS |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier |
1 |