Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Entire neuroepithelial layer |
Is a |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
|
Rod of retina |
partie de |
False |
Neuroepithelial layer |
Inferred relationship |
Some |
|
Cone of retina |
partie de |
False |
Neuroepithelial layer |
Inferred relationship |
Some |
|
Central serous retinopathy with pit of optic disc |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
2 |
Chronic central serous chorioretinopathy |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
2 |
Inactive central serous chorioretinopathy |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
2 |
Acute central serous chorioretinopathy |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
2 |
Central serous chorioretinopathy (disorder) |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
2 |
Variant central serous chorioretinopathy |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
2 |
Acute central serous retinopathy with subretinal fluid |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
2 |
Chronic central serous retinopathy with diffuse retinal pigment epithelial detachment |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
2 |
Inactive central serous retinopathy with focal retinal pigment epithelial detachment |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
3 |
Central serous retinopathy with small retinal pigment epithelial detachment |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
3 |
Serous macular detachment (disorder) |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
2 |
Serous retinal detachment |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
2 |
Structure of neuroepithelial layer of retina of left eye (body structure) |
Is a |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
|
Structure of neuroepithelial layer of retina of right eye (body structure) |
Is a |
True |
Neuroepithelial layer |
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. |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
1 |
A rare genetic isolated inherited retinal disorder characterised by primary cone degeneration with significant secondary rod involvement, with a variable fundus appearance. Typical presentation includes decreased visual acuity, central scotoma, photophobia, colour vision alteration, followed by night blindness and loss of peripheral visual field. |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
1 |
Adenoma of neuroepithelium of iris |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
1 |
Serous detachment of retinal pigment epithelium |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
2 |
Serous detachment of right retinal pigment epithelium (disorder) |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
2 |
Serous detachment of left retinal pigment epithelium |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
2 |
Serous detachment of bilateral retinal pigment epithelium (disorder) |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
3 |
Primary adenocarcinoma of iris neuroepithelium |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
1 |
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. |
Finding site |
True |
Neuroepithelial layer |
Inferred relationship |
Some |
1 |