MYP11
MCID: MYP143
MIFTS: 15

Myopia 11, Autosomal Dominant (MYP11)

Categories: Eye diseases, Genetic diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Myopia 11, Autosomal Dominant

MalaCards integrated aliases for Myopia 11, Autosomal Dominant:

Name: Myopia 11, Autosomal Dominant 57
Myopia 11 57 13 70
Myp11 57

Classifications:



External Ids:

OMIM® 57 609994
OMIM Phenotypic Series 57 PS160700
MedGen 41 C1864941
UMLS 70 C1864941

Summaries for Myopia 11, Autosomal Dominant

OMIM® : 57 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 blurry and near objects are clear (summary by Kaiser et al., 2004). For a discussion of genetic heterogeneity of susceptibility to myopia, see 160700. (609994) (Updated 20-May-2021)

MalaCards based summary : Myopia 11, Autosomal Dominant, also known as myopia 11, is related to myopia. An important gene associated with Myopia 11, Autosomal Dominant is MYP11 (Myopia 11 (High Grade, Autosomal Dominant)). Affiliated tissues include eye and retina.

Related Diseases for Myopia 11, Autosomal Dominant

Symptoms & Phenotypes for Myopia 11, Autosomal Dominant

Clinical features from OMIM®:

609994 (Updated 20-May-2021)

Drugs & Therapeutics for Myopia 11, Autosomal Dominant

Search Clinical Trials , NIH Clinical Center for Myopia 11, Autosomal Dominant

Genetic Tests for Myopia 11, Autosomal Dominant

Anatomical Context for Myopia 11, Autosomal Dominant

MalaCards organs/tissues related to Myopia 11, Autosomal Dominant:

40
Eye, Retina

Publications for Myopia 11, Autosomal Dominant

Articles related to Myopia 11, Autosomal Dominant:

(show all 11)
# Title Authors PMID Year
1
A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612. 57
16052171 2005
2
Five-year incidence of visual impairment and blindness in adult Chinese the Beijing Eye Study. 61
21211839 2011
3
A functional polymorphism at 3'UTR of the PAX6 gene may confer risk for extreme myopia in the Chinese. 61
21421876 2011
4
Short-term efficacy and safety of intravitreal ranibizumab for myopic choroidal neovascularization. 61
18788102 2008
5
Relation of pre-LASIK and post-LASIK retinal lesions and retinal examination for LASIK eyes. 61
15722308 2005
6
Laser-assisted subepithelial keratectomy in children. 61
15617920 2004
7
Phototherapeutic keratectomy in children: 5-year results. 61
15342054 2004
8
Subretinal surgery for juxtafoveal choroidal neovascularization. 61
12972755 2003
9
Influence of temperature and humidity on laser in situ keratomileusis outcomes. 61
11316022 2001
10
Initial experience of inferior limited macular translocation for subfoveal choroidal neovascularization resulting from causes other than age-related macular degeneration. 61
11162983 2001
11
Holmium laser thermokeratoplasty for the reversal of hyperopia after myopic photorefractive keratectomy. 61
9290364 1997

Variations for Myopia 11, Autosomal Dominant

Expression for Myopia 11, Autosomal Dominant

Search GEO for disease gene expression data for Myopia 11, Autosomal Dominant.

Pathways for Myopia 11, Autosomal Dominant

GO Terms for Myopia 11, Autosomal Dominant

Sources for Myopia 11, Autosomal Dominant

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 20-May-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
Content
Loading form....