Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Optic nerve and pathway injury |
Is a |
False |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Disorder of optic radiation |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Disorder of visual cortex |
Is a |
False |
Disorder of visual pathways |
Inferred relationship |
Some |
|
forstyrrelse af synsbaner associeret med inflammatorisk sygdom |
Is a |
False |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Disorder of visual pathways associated with vascular disorder |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Optic chiasm disorder (disorder) |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Disorder of visual pathways associated with neoplasm |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Disorder of optic nerve |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Disorder of optic tract |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Visual pathway disorder due to neoplasm (disorder) |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Visual pathway disorder due to vascular disorder |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
andre lidelser i nervus opticus |
Is a |
False |
Disorder of visual pathways |
Inferred relationship |
Some |
|
anden synsbanesygdom |
Is a |
False |
Disorder of visual pathways |
Inferred relationship |
Some |
|
sygdom i nervus opticus eller synsbane, ikke nærmere specificeret |
Is a |
False |
Disorder of visual pathways |
Inferred relationship |
Some |
|
[X]Optic atrophy in diseases classified elsewhere |
Is a |
False |
Disorder of visual pathways |
Inferred relationship |
Some |
|
[X]Retrobulbar neuritis in diseases classified elsewhere |
Is a |
False |
Disorder of visual pathways |
Inferred relationship |
Some |
|
[X]Other disorders of optic nerve and visual pathways in diseases classified elsewhere |
Is a |
False |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Tobacco amblyopia |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Malignant neoplasm of optic nerve sheath (disorder) |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Meningioma of optic nerve sheath (disorder) |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Nerve fiber bundle defect |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Riddoch phenomenon (disorder) |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Traumatic injury of visual pathways |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Glioma opticum |
Is a |
False |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Nerve fibre layer infarct |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Central serous chorioretinopathy |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Serous retinal detachment |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
A rare syndromic intellectual disability syndrome with characteristics of cortical blindness, different types of seizures, intellectual disability with limited or absent speech and dysmorphic facial features. Brain imaging typically shows mild pontine hypoplasia, hypoplasia of the corpus callosum and atrophy in the occipital region. There is evidence the disease is caused by compound heterozygous mutation in the DOCK7 gene on chromosome 1p31. |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Inflammatory disorder of visual pathway (disorder) |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by congenital, total, cortical blindness, intellectual disability, postaxial polydactyly of the hands and feet, pre- and postnatal growth delay, psychomotor developmental retardation, and mild facial dysmorphism (including prominent forehead, short nose, long philtrum, high-arched palate, and microretrognathia). Recurrent respiratory and intestinal infections, as well as moderate hypertonia and hyperreflexia, are also associated. There have been no further descriptions in the literature since 1985. |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Bilateral cortical blindness of brain |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Malignant optic glioma (disorder) |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Hemorrhage in optic nerve sheaths |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
A rare retinal dystrophy with characteristics of photophobia, progressive loss of visual acuity, nystagmus, visual field abnormalities, abnormal color vision, and psychophysical and electrophysiological evidence of abnormal cone function. Progressive cone dystrophy usually presents in childhood or early adult life, and patients tend to develop rod photoreceptor dysfunction in later life. |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Adenoma of neuroepithelium of iris |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome is characterized by the association of spondylometaphyseal dysplasia (marked by platyspondyly, shortening of the tubular bones and progressive metaphyseal irregularity and cupping), with postnatal growth retardation and progressive visual impairment due to cone-rod dystrophy. So far, it has been described in eight individuals. Transmission appears to be autosomal recessive. |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Primary adenocarcinoma of iris neuroepithelium |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
A rare genetic systemic or rheumatologic disease characterized by infantile onset of skin anomalies (such as delayed wound healing with atrophic scars and mild alopecia with dry and brittle hair), retinal rod degeneration with night blindness, degenerative myopathy with muscle weakness, myalgia, and cramps, osteoarthritis, joint laxity, prolapse of internal organs, floating kidney syndrome, malabsorption syndrome, and hypothyroidism. The phenotype has been reported to be more severe in women than in men. |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Cyst of optic nerve sheath (disorder) |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|
Myelinated nerve fiber layer of retina |
Is a |
True |
Disorder of visual pathways |
Inferred relationship |
Some |
|