MACULAR DYSTROPHY, VITELLIFORM, 5

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 6
OrphanetNr:
OMIM Id: 616152
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0007754) Macular dystrophy 26 / 7739
2
 (HPO:0007663) Reduced visual acuity 100 / 7739
3
 (HPO:0000603) Central scotoma 18 / 7739
4
 (HPO:0007677) Vitelliform-like macular lesions 4 / 7739
5
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739
6
 (HPO:0030515) Moderate visual impairment 2 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: