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Summary Literature (0)
DOID:11830 - myopia


Disease Ontology Definition:A refractive error characterized by the inability to see farther objects clearly.

Synonyms: near-sightedness, near vision, short-sightedness

Xenbase Genes : sco2, lrpap1, slc39a5, znf644, primpol

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0001384 - primary motor cortex

MIM:
MIM:160700 - MYOPIA 2, AUTOSOMAL DOMINANT; MYP2
MIM:255500 - MYOPIA 18, AUTOSOMAL RECESSIVE; MYP18
MIM:300613 - MYOPIA 13, X-LINKED; MYP13
MIM:310460 - MYOPIA 1, X-LINKED; MYP1
MIM:603221 - MYOPIA 3, AUTOSOMAL DOMINANT; MYP3
MIM:608367 - MYOPIA 17, AUTOSOMAL DOMINANT; MYP17
MIM:608474 - MYOPIA 5, AUTOSOMAL DOMINANT; MYP5
MIM:608908 - MYOPIA 6; MYP6
MIM:609256 - MYOPIA 7; MYP7
MIM:609257 - MYOPIA 8; MYP8
MIM:609258 - MYOPIA 9; MYP9
MIM:609259 - MYOPIA 10; MYP10
MIM:609994 - MYOPIA 11, AUTOSOMAL DOMINANT; MYP11
MIM:609995 - MYOPIA 12, AUTOSOMAL DOMINANT; MYP12
MIM:610320 - MYOPIA 14; MYP14
MIM:612554 - MYOPIA 16, AUTOSOMAL DOMINANT; MYP16
MIM:612717 - MYOPIA 15, AUTOSOMAL DOMINANT; MYP15
MIM:613959 - SCHIZOPHRENIA 16; SCZD16
MIM:613969 - MYOPIA 19, AUTOSOMAL DOMINANT; MYP19
MIM:614166 - MYOPIA 20, AUTOSOMAL DOMINANT; MYP20
MIM:614167 - MYOPIA 21, AUTOSOMAL DOMINANT; MYP21
MIM:615420 - MYOPIA 22, AUTOSOMAL DOMINANT; MYP22
MIM:615431 - MYOPIA 23, AUTOSOMAL RECESSIVE; MYP23
MIM:615946 - MYOPIA 24, AUTOSOMAL DOMINANT; MYP24

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): refractive error (is_a)