MYP14
MCID: MYP069
MIFTS: 15

Myopia 14 (MYP14)

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

Aliases & Classifications for Myopia 14

MalaCards integrated aliases for Myopia 14:

Name: Myopia 14 56 13 71
Myp14 56

Classifications:



External Ids:

OMIM 56 610320
OMIM Phenotypic Series 56 PS160700
MedGen 41 C1853196
UMLS 71 C1853196

Summaries for Myopia 14

OMIM : 56 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. (610320)

MalaCards based summary : Myopia 14, also known as myp14, is related to myopia. An important gene associated with Myopia 14 is MYP14 (Myopia 14). Affiliated tissues include retina and eye.

Related Diseases for Myopia 14

Symptoms & Phenotypes for Myopia 14

Clinical features from OMIM:

610320

Drugs & Therapeutics for Myopia 14

Search Clinical Trials , NIH Clinical Center for Myopia 14

Genetic Tests for Myopia 14

Anatomical Context for Myopia 14

MalaCards organs/tissues related to Myopia 14:

40
Retina, Eye

Publications for Myopia 14

Articles related to Myopia 14:

(show all 11)
# Title Authors PMID Year
1
Genomewide scan in Ashkenazi Jewish families demonstrates evidence of linkage of ocular refraction to a QTL on chromosome 1p36. 56
16501916 2006
2
Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12. 56
15273935 2004
3
Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families. 61
30704416 2019
4
Variation of choroidal thickness and vessel diameter in patients with posterior non-infectious uveitis. 61
26530342 2014
5
Morphometric characteristics of optic disc in patients with myopia and primary open-angle glaucoma. 61
23401930 2013
6
An international collaborative family-based whole genome quantitative trait linkage scan for myopic refractive error. 61
22509102 2012
7
An international collaborative family-based whole-genome linkage scan for high-grade myopia. 61
19324860 2009
8
Incidence of ocular pathologies in Italian children with Down syndrome. 61
17932861 2007
9
Ocular abnormalities in Apert syndrome: genotype/phenotype correlations with fibroblast growth factor receptor type 2 mutations. 61
17189145 2006
10
Long-term results after scleral buckling surgery in uncomplicated juvenile retinal detachment without proliferative vitreoretinopathy. 61
9869456 1998
11
Retinal detachment after clear lens extraction in 41 eyes with high axial myopia. 61
8927807 1996

Variations for Myopia 14

Expression for Myopia 14

Search GEO for disease gene expression data for Myopia 14.

Pathways for Myopia 14

GO Terms for Myopia 14

Sources for Myopia 14

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
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
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
Content
Loading form....