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1 OMIM reference -
3 associated genes
10 signs/symptoms
PROTEIN INTERACTIONS: 1
2 associated genes
No signs/symptoms info
Adult-onset foveomacular vitelliform dystrophy
Acute myelomonocytic leukemia

BEST1 FLT3
IMPG1 NPM1
PRPH2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
IMPG1
(0.63)
NPM1



Citations in the biomedical literature:


Adult-onset foveomacular vitelliform dystrophy
BEST1 IMPG1 PRPH2
Acute myelomonocytic leukemia
FLT3 NPM1



Adult-onset foveomacular vitelliform dystrophy
Acute myelomonocytic leukemia

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

Synonym(s):
(no synonyms)

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

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
1 MeSH reference: D015479

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


Acute myelomonocytic leukemia

(no data available)