MYP20
MCID: MYP084
MIFTS: 12

Myopia 20, Autosomal Dominant (MYP20)

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

Aliases & Classifications for Myopia 20, Autosomal Dominant

MalaCards integrated aliases for Myopia 20, Autosomal Dominant:

Name: Myopia 20, Autosomal Dominant 57 13 70
Myp20 57

Classifications:



External Ids:

OMIM® 57 614166
OMIM Phenotypic Series 57 PS160700
UMLS 70 C3279996

Summaries for Myopia 20, 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. (614166) (Updated 20-May-2021)

MalaCards based summary : Myopia 20, Autosomal Dominant, is also known as myp20. An important gene associated with Myopia 20, Autosomal Dominant is MYP20 (Myopia 20, Autosomal Dominant). Affiliated tissues include eye and retina.

Related Diseases for Myopia 20, Autosomal Dominant

Symptoms & Phenotypes for Myopia 20, Autosomal Dominant

Clinical features from OMIM®:

614166 (Updated 20-May-2021)

Drugs & Therapeutics for Myopia 20, Autosomal Dominant

Search Clinical Trials , NIH Clinical Center for Myopia 20, Autosomal Dominant

Genetic Tests for Myopia 20, Autosomal Dominant

Anatomical Context for Myopia 20, Autosomal Dominant

MalaCards organs/tissues related to Myopia 20, Autosomal Dominant:

40
Eye, Retina

Publications for Myopia 20, Autosomal Dominant

Articles related to Myopia 20, Autosomal Dominant:

# Title Authors PMID Year
1
Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population. 57
21640322 2011

Variations for Myopia 20, Autosomal Dominant

Expression for Myopia 20, Autosomal Dominant

Search GEO for disease gene expression data for Myopia 20, Autosomal Dominant.

Pathways for Myopia 20, Autosomal Dominant

GO Terms for Myopia 20, Autosomal Dominant

Sources for Myopia 20, 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
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