MYP9
MCID: MYP048
MIFTS: 17

Myopia 9 (MYP9)

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

Aliases & Classifications for Myopia 9

MalaCards integrated aliases for Myopia 9:

Name: Myopia 9 56 13 71
Myp9 56

Characteristics:

OMIM:

56
Inheritance:
multifactorial


Classifications:



External Ids:

OMIM 56 609258
OMIM Phenotypic Series 56 PS160700
MedGen 41 C1836504
SNOMED-CT via HPO 68 57190000
UMLS 71 C1836504

Summaries for Myopia 9

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. (609258)

MalaCards based summary : Myopia 9, also known as myp9, is related to myopia. An important gene associated with Myopia 9 is MYP9 (Myopia 9). Affiliated tissues include retina and eye, and related phenotype is myopia.

Related Diseases for Myopia 9

Symptoms & Phenotypes for Myopia 9

Human phenotypes related to Myopia 9:

31
# Description HPO Frequency HPO Source Accession
1 myopia 31 HP:0000545

Symptoms via clinical synopsis from OMIM:

56
Head And Neck Eyes:
myopia, low to moderate (-12.12 d to +7.25 d)

Clinical features from OMIM:

609258

Drugs & Therapeutics for Myopia 9

Search Clinical Trials , NIH Clinical Center for Myopia 9

Genetic Tests for Myopia 9

Anatomical Context for Myopia 9

MalaCards organs/tissues related to Myopia 9:

40
Retina, Eye

Publications for Myopia 9

Articles related to Myopia 9:

(show all 11)
# Title Authors PMID Year
1
A susceptibility locus for myopia in the normal population is linked to the PAX6 gene region on chromosome 11: a genomewide scan of dizygotic twins. 56
15307048 2004
2
Visual impairment and amblyopia in Malaysian pre-school children - The SEGPAEDS study. 61
29531199 2018
3
Intravitreal ziv-aflibercept for the treatment of choroidal neovascularisation associated with conditions other than age-related macular degeneration. 61
28119292 2017
4
Macular Pigment Optical Density and Ocular Pulse Amplitude in Subjects with Different Axial Lengths and Refractive Errors. 61
26071973 2015
5
Refractive errors in presbyopic patients in Kano, Nigeria. 61
24521573 2014
6
Intravitreal bevacizumab for retinopathy of prematurity: refractive error results. 61
23490192 2013
7
Genomewide linkage scans for ocular refraction and meta-analysis of four populations in the Myopia Family Study. 61
19151385 2009
8
Ocular abnormalities in Apert syndrome: genotype/phenotype correlations with fibroblast growth factor receptor type 2 mutations. 61
17189145 2006
9
Morphologic and angiographic assessment of the macula after macular translocation surgery with 360 degrees retinotomy. 61
14644725 2003
10
A retrospective study of low-vision cases in an Indian tertiary eye-care hospital. 61
11217251 2000
11
[Aberrometry in the diagnosis of eye diseases]. 61
2095474 1990

Variations for Myopia 9

Expression for Myopia 9

Search GEO for disease gene expression data for Myopia 9.

Pathways for Myopia 9

GO Terms for Myopia 9

Sources for Myopia 9

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
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