ODCs

Click node...

1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
3 associated genes
10 signs/symptoms

Retinopathy, Burgess-Black type

Adult-onset foveomacular vitelliform dystrophy

Citations in the biomedical literature:

Retinopathy, Burgess-Black type		Adult-onset foveomacular vitelliform dystrophy
	Synonym(s): - Autosomal recessive bestrophinopathy		Synonym(s): - AOFMD - AVMD - Adult-onset foveomacular dystrophy - Adult-onset foveomacular dystrophy with choroidal neovascularization - Adult-onset vitelliform macular dystrophy - Gass disease - Pseudo-Best disease - Pseudo-vitelliform macular dystrophy

	Classification (Orphanet): - Rare eye disease - Rare genetic disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease

	Classification (ICD10): - Diseases of the eye and adnexa -		Classification (ICD10): - Diseases of the eye and adnexa -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: any age Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: normal Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - No MeSH references

Adult-onset foveomacular vitelliform dystrophy
	Very frequent - Anomalies of eyes and vision - Autosomal dominant inheritance - Macular dystrophy / absence / hypoplasia of the macula - Mild visual loss / impaired visual acuity Frequent - Abnormal visual field / hemianopsia / hemianopia / scotoma / visual peripheral rim - Achromatopsia / dyschromatopsia / daltonism / impaired colour vision - Choroidal anomalies / atrophy / choroideremia - Retinitis pigmentosa / retinal pigmentary changes Occasional - Retinal detachment - Visual loss / blindness / amblyopia
Retinopathy, Burgess-Black type
(no data available)