Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Macular retinoschisis |
Is a |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Occult neovascularisation of macula |
Is a |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Forster-Fuchs' spot (disorder) |
Is a |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Age related macular degeneration |
Is a |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Myopic macular degeneration (disorder) |
Is a |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Cystoid macular retinal degeneration |
Is a |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Fundus flavimaculatus |
Is a |
False |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
familiær pseudoinflammatorisk maculadegeneration |
Is a |
False |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Degeneration af macula og bageste linsepol |
Is a |
False |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Degeneration of macula due to cyst, hole or pseudohole |
Is a |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Family history of degenerative disorder of macula (situation) |
Associated finding |
False |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
1 |
Stargardt's disease |
Is a |
False |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Family history of degenerative disorder of macula (situation) |
Associated finding |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
1 |
Family history of degenerative disorder of macula (situation) |
Associated finding |
False |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
1 |
Hypotrichosis with juvenile macular degeneration (HJMD) is a very rare syndrome characterized by sparse and short hair from birth followed by progressive macular degeneration leading to blindness. |
Is a |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
History of macular degeneration |
Associated finding |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
1 |
Hereditary macular dystrophy |
Is a |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Macular pigment deposit |
Is a |
False |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Macular vitelliform deposits |
Is a |
False |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Knobloch syndrome is defined by vitreoretinal and macular degeneration, and occipital encephalocele. The disease has characteristics of early-onset severe myopia (usually becoming apparent in the first year of life), vitreoretinal degeneration with retinal detachment, macular abnormalities, and midline encephalocele (mainly in the occipital region). The syndrome is clinically and genetically heterogeneous with three forms, KNO1, KNO2 and KNO3, being defined. KNO1 is caused by inactivating mutations in the collagen XVIII/endostatin gene (COL18A1) mapped to 21q22.3. The KNO2 form was defined when linkage to the KNO1 locus was excluded in a family reported from New Zealand. Recently, a novel type of KS (KNO3) was mapped to chromosome 17q11.2. Inherited as an autosomal recessive trait. |
Is a |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Persistent placoid maculopathy is characterized by white plaque-like lesions involving the macula but sparing the peripapillary areas of both eyes. It has been described in five patients. In contrast to patients with macular serpiginous choroiditis presenting with similar lesions, the five patients reported so far with persistent placoid maculopathy had good visual acuity until the onset of choroidal neovascularization (CNV) or pigmentary mottling. The macular lesions fade after several months or years, but the vascular anomalies persist leading to a loss of central vision. |
Is a |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Atrophy of macula lutea |
Is a |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Macular exudate (disorder) |
Is a |
False |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Myopic foveoschisis |
Is a |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
A disorder characterized by the presence of RPE (retinal pigment epithelium) disruption within the posterior pole over regions of choroidal thickening in eyes, showing no evidence of active or prior CSC (central serous chorioretinopathy). |
Is a |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
Best vitelliform macular dystrophy (BVMD) is a genetic macular dystrophy characterized by loss of central visual acuity, metamorphopsia and a decrease in the Arden ratio secondary to an egg yolk-like lesion located in the foveal or parafoveal region. |
Is a |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|
A rare genetic macular dystrophy with characteristics of blurred vision, metamorphopsia and mild visual impairment secondary to a slightly elevated yellow egg yolk-like lesion located in the foveal or parafoveal region. Clinical onset is typically between the fourth and sixth decade of life. The mechanism underlying the physiopathology is unknown. An autosomal dominant inheritance with variable expression and incomplete penetrance is suggested but the disease can also be sporadic without evidence of a familial inheritance pattern. |
Is a |
True |
Degenerative disorder of macula (disorder) |
Inferred relationship |
Some |
|