MYP7
MCID: MYP040
MIFTS: 15

Myopia 7 (MYP7)

Categories: Eye diseases, Genetic diseases, Rare diseases

Aliases & Classifications for Myopia 7

MalaCards integrated aliases for Myopia 7:

Name: Myopia 7 58 13 74
Myp7 58

Characteristics:

OMIM:

58
Inheritance:
multifactorial


Classifications:



External Ids:

OMIM 58 609256
MedGen 43 C1836506
SNOMED-CT via HPO 70 57190000
UMLS 74 C1836506

Summaries for Myopia 7

OMIM : 58 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. (609256)

MalaCards based summary : Myopia 7, also known as myp7, is related to myopia and cone-rod dystrophy and hearing loss 2. An important gene associated with Myopia 7 is MYP7 (Myopia 7). Affiliated tissues include retina and eye, and related phenotype is myopia.

Related Diseases for Myopia 7

Symptoms & Phenotypes for Myopia 7

Human phenotypes related to Myopia 7:

33
# Description HPO Frequency HPO Source Accession
1 myopia 33 HP:0000545

Symptoms via clinical synopsis from OMIM:

58
Head And Neck Eyes:
myopia, low to moderate (-12.12 d to +7.25 d)

Clinical features from OMIM:

609256

Drugs & Therapeutics for Myopia 7

Search Clinical Trials , NIH Clinical Center for Myopia 7

Genetic Tests for Myopia 7

Anatomical Context for Myopia 7

MalaCards organs/tissues related to Myopia 7:

42
Retina, Eye

Publications for Myopia 7

Variations for Myopia 7

Expression for Myopia 7

Search GEO for disease gene expression data for Myopia 7.

Pathways for Myopia 7

GO Terms for Myopia 7

Sources for Myopia 7

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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