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Coats disease
1 OMIM reference -
1 associated gene
19 connected diseases
9 signs/symptoms
Disease Type of connection
Familial exudative vitreoretinopathy
Retinopathy of prematurity
Persistent hyperplastic primary vitreous
Norrie disease
Autosomal dominant osteopetrosis type 1
Autosomal dominant osteosclerosis, Worth type
Familial isolated dilated cardiomyopathy
Hyperostosis corticalis generalisata
Idiopathic juvenile osteoporosis
Muscular dystrophy, Selcen type
Osteoporosis - pseudoglioma
Osteosclerosis - developmental delay - craniosynostosis
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Synonym(s):
- Congenital retinal telangiectasia
- Leber miliary aneurysm
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the eye and adnexa -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: normal
Type of inheritance: sporadic
External references:
1 OMIM reference -
1 MeSH reference: D058456
Gene symbol UniProt reference OMIM reference
NDP Q00604300658
Very frequent
- Retinal vascular anomalies / retinal telangiectasia
- Strabismus / squint

Frequent
- Glaucoma
- Macular dystrophy / absence / hypoplasia of the macula
- Retinal detachment

Occasional
- Aniridia / iris hypoplasia
- Anterior chamber anomaly
- Cataract / lens opacification
- Visual loss / blindness / amblyopia