MYP19
MCID: MYP147
MIFTS: 16

Myopia 19, Autosomal Dominant (MYP19)

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

Aliases & Classifications for Myopia 19, Autosomal Dominant

MalaCards integrated aliases for Myopia 19, Autosomal Dominant:

Name: Myopia 19, Autosomal Dominant 56 13 71
Myopia 19 56
Myp19 56

Characteristics:

OMIM:

56
Inheritance:
autosomal dominant


HPO:

31
myopia 19, autosomal dominant:
Inheritance autosomal dominant inheritance


Classifications:



External Ids:

OMIM 56 613969
OMIM Phenotypic Series 56 PS160700
MedGen 41 C3151410
SNOMED-CT via HPO 68 263681008 34187009
UMLS 71 C3151410

Summaries for Myopia 19, Autosomal Dominant

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. (613969)

MalaCards based summary : Myopia 19, Autosomal Dominant, is also known as myopia 19. An important gene associated with Myopia 19, Autosomal Dominant is MYP19 (Myopia 19, Autosomal Dominant). Affiliated tissues include retina and eye, and related phenotype is high myopia.

Related Diseases for Myopia 19, Autosomal Dominant

Symptoms & Phenotypes for Myopia 19, Autosomal Dominant

Human phenotypes related to Myopia 19, Autosomal Dominant:

31
# Description HPO Frequency HPO Source Accession
1 high myopia 31 HP:0011003

Symptoms via clinical synopsis from OMIM:

56
Head And Neck Eyes:
high myopia

Clinical features from OMIM:

613969

Drugs & Therapeutics for Myopia 19, Autosomal Dominant

Search Clinical Trials , NIH Clinical Center for Myopia 19, Autosomal Dominant

Genetic Tests for Myopia 19, Autosomal Dominant

Anatomical Context for Myopia 19, Autosomal Dominant

MalaCards organs/tissues related to Myopia 19, Autosomal Dominant:

40
Retina, Eye

Publications for Myopia 19, Autosomal Dominant

Articles related to Myopia 19, Autosomal Dominant:

# Title Authors PMID Year
1
Identification of a locus for autosomal dominant high myopia on chromosome 5p13.3-p15.1 in a Chinese family. 56
21042559 2010
2
Visual performance after implantation of two types of phakic foldable intraocular lenses for correction of high myopia. 61
30809486 2019
3
Posterior scleral reinforcement using genipin-cross-linked sclera for macular hole retinal detachment in highly myopic eyes. 61
29519878 2018
4
[Clinical observation on corneal transparency after small incision lenticule extraction surgery]. 61
29429284 2018
5
Macular Pigment Optical Density and Ocular Pulse Amplitude in Subjects with Different Axial Lengths and Refractive Errors. 61
26071973 2015
6
[Ocular refraction in Zaire]. 61
9035823 1996
7
Myopia and plasma cortisol. 61
2583791 1989

Variations for Myopia 19, Autosomal Dominant

Expression for Myopia 19, Autosomal Dominant

Search GEO for disease gene expression data for Myopia 19, Autosomal Dominant.

Pathways for Myopia 19, Autosomal Dominant

GO Terms for Myopia 19, Autosomal Dominant

Sources for Myopia 19, Autosomal Dominant

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....