Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Intraocular optic nerve glioma (disorder) |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Neoplasm of uncertain behavior of optic nerve |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary optic atrophy |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Paraneoplastic optic neuropathy (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Excision of lesion of optic nerve (II) |
Procedure site - Direct (attribute) |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Repair of optic nerve (II) |
Procedure site - Direct (attribute) |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Compressive optic atrophy |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary malignant neoplasm of optic nerve (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dominant hereditary optic atrophy |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Optic atrophy associated with retinal dystrophy |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Injection of optic nerve |
Procedure site - Indirect (attribute) |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Secondary optic atrophy |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Optic atrophy secondary to retinal disease |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Foster-Kennedy syndrome (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hereditary optic atrophy (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Optic atrophy |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Exploration of optic nerve (II) (procedure) |
Procedure site - Direct (attribute) |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Radial optic neurotomy |
Procedure site - Direct (attribute) |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Optic nerve glioma (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Benign neoplasm of optic nerve (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Optic neuritis |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Malignant optic glioma (disorder) |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Compressive optic neuropathy due to thyroid eye disease (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hereditary optic atrophy NOS |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Strahlenschäden des Sehnervs |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Intracranial transection of optic nerve (II) |
Procedure site - Direct (attribute) |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Incipient prechiasmal optic nerve compression syndrome |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Intracranial stereotactic neurolysis of optic nerve (II) (procedure) |
Procedure site - Direct (attribute) |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Wolfram syndrome (disorder) |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Endoscopy of nasal sinus with decompression of optic nerve (procedure) |
Procedure site - Direct (attribute) |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Endoscopy of nasal sinus with decompression of optic nerve (procedure) |
Procedure site - Direct (attribute) |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Endoscopic decompression of optic nerve |
Procedure site - Direct (attribute) |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Endoscopic decompression of optic nerve |
Procedure site - Direct (attribute) |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Septo-optic dysplasia sequence |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Hypoplasia of the optic nerve |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Partial hypoplasia of optic disc (disorder) |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Congenital anomaly of optic nerve |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Malignant optic glioma (disorder) |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Malignant optic glioma of adulthood |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Autosomal dominant optic atrophy plus syndrome (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Oculocerebral dysplasia syndrome |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Autosomal dominant optic atrophy classic form (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autosomal dominant optic atrophy and peripheral neuropathy syndrome (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Behr syndrome |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
A rare inherited mitochondrial disease characterized by the clinical features of Leber hereditary optic neuropathy in combination with other systemic or neurological abnormalities. These abnormalities include postural tremor, motor disorder, multiple sclerosis-like syndrome, spinal cord disease, skeletal changes, Parkinsonism with dystonia, anarthria, motor and sensory peripheral neuropathy, spasticity, mild encephalopathy, and cardiac arrhythmias. |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Autosomal dominant optic atrophy and cataract (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Optic neuropathy due to folate deficiency (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Infection causing inflammation of optic nerve (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Early-onset X-linked optic atrophy (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Disorder of optic nerve due to and following radiotherapy (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder) |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Meningococcal optic neuritis |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Severe X-linked intellectual disability Gustavson type (disorder) |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Aplasia of optic nerve (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital atrophy of optic nerve (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Perioperative secondary non-arteritic ischemic optic neuropathy (disorder) |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
X-linked spastic paraplegia type 2 (disorder) |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Structure of left optic nerve (body structure) |
Is a |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Structure of right optic nerve (body structure) |
Is a |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder) |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
A disorder that is characterized by the association of a non-progressive congenital ataxia, severe intellectual deficit, optic atrophy and structural anomalies of the skin vessels. It has been described in five children from a large consanguineous Lebanese family. Short stature and microcephaly were also reported. Transmission is autosomal recessive. |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Isolated hypoplasia of optic nerve (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Malignant optic glioma of adulthood |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ischemic optic neuropathy |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Arteritic ischemic optic neuropathy |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Non-arteritic ischemic optic neuropathy |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Anterior ischemic optic neuropathy (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Posterior ischemic optic neuropathy |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Perioperative secondary non-arteritic ischemic optic neuropathy (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Arteritic anterior ischemic optic neuropathy (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Wolfram-like syndrome |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Combined immunodeficiency with faciooculoskeletal anomalies syndrome (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Optic atrophy, intellectual disability syndrome |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
A rare genetic syndrome with characteristics of severe developmental delay, neonatal hypotonia, seizures, optic nerve hypoplasia and distinct central nervous system malformations including extensive bilateral polymicrogyria, dysplastic or absent corpus callosum and malformed brainstem with loss of demarcation of the pontomedullary junction. There is evidence this disease is caused by homozygous mutation in the TUBA8 gene on chromosome 22q11. |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Optic nerve edema, splenomegaly syndrome |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Severe X-linked intellectual disability Gustavson type (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Oculocerebral dysplasia syndrome |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Septo-optic dysplasia sequence |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A disorder that is characterized by the association of a non-progressive congenital ataxia, severe intellectual deficit, optic atrophy and structural anomalies of the skin vessels. It has been described in five children from a large consanguineous Lebanese family. Short stature and microcephaly were also reported. Transmission is autosomal recessive. |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Infantile cerebellar and retinal degeneration (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Autosomal recessive optic atrophy type 7 (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Alcohol related optic neuropathy |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Fatal X-linked ataxia with deafness and loss of vision (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Neuromyelitis optica |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autosomal recessive spastic paraplegia type 55 (disorder) |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Autosomal recessive spastic paraplegia type 57 |
Finding site |
False |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
SPOAN and SPOAN-related disorder |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Arteritic anterior ischemic optic neuropathy due to giant cell arteritis (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autosomal recessive optic atrophy type 6 (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autoimmune optic neuropathy (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Childhood-onset autosomal dominant optic atrophy (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Idiopathic non-arteritic posterior ischemic optic neuropathy (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Idiopathic non-arteritic ischaemic optic neuropathy |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Optic atrophy due to late syphilis (disorder) |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hypoplasia of optic nerve due to central nervous system malformation |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Optic nerve hypoplasia due to endocrine deficiency |
Finding site |
True |
Optic nerve structure |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |