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Adult-onset foveomacular vitelliform dystrophy
1 OMIM reference -
3 associated genes
15 connected diseases
10 signs/symptoms
Disease Type of connection
Retinitis pigmentosa
Autosomal dominant vitreoretinochoroidopathy
Best vitelliform macular dystrophy
Butterfly-shaped pigment dystrophy
Central areolar choroidal dystrophy
Cone rod dystrophy
Fundus albipunctatus
MRCS syndrome
Retinitis punctata albescens
Retinopathy, Burgess-Black type
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Acute promyelocytic leukemia
Amyotrophic lateral sclerosis
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 (ICD10):
- Diseases of the eye and adnexa -
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
Gene symbol UniProt reference OMIM reference
BEST1 O76090607854
IMPG1 Q17R60602870
PRPH2 P23942179605
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