MYOPIA 17, AUTOSOMAL DOMINANT

General Information (adopted from Orphanet):

Synonyms, Signs: MYP4, FORMERLY
MYOPIA 4, FORMERLY
MYP17
Number of Symptoms 7
OrphanetNr:
OMIM Id: 608367
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0007819) Presenile cataracts 5 / 7739
2
 (HPO:0011530) Retinal hole 3 / 7739
3
 (HPO:0011003) Severe Myopia 31 / 7739
4
 (OMIM) Myopia, high-grade bilateral (range -5.50 to -50 diopters, average adult refractive error -13.925 diopters) 1 / 7739
5
 (OMIM) Multiple retinal holes 1 / 7739
6
 (OMIM) Increased ocular axial length (35 mm vs. 24 mm in normal non-myopes) 1 / 7739
7
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information:

Description: (OMIM) Myopia, or nearsightedness, is a refractive error of the eye. Light rays from a distant object are focused in front of the retina and those from a near object are focused in the retina; therefore distant objects are ...