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Summary Literature (0)
DOID:4428 - dyslexia

Disease Ontology Definition:A reading disorder resulting from a developmental reading disability involving the inability to process graphic symbols resulting in impairment of reading ability.

Synonyms:

Xenbase Genes : dcdc2, KIAA0319

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0005489 - dyslexia

MIM:
MIM:300509 - DYSLEXIA, SUSCEPTIBILITY TO, 9; DYX9
MIM:600202 - DYSLEXIA, SUSCEPTIBILITY TO, 2; DYX2
MIM:604254 - DYSLEXIA, SUSCEPTIBILITY TO, 3; DYX3
MIM:606616 - DYSLEXIA, SUSCEPTIBILITY TO, 6; DYX6
MIM:606896 - DYSLEXIA, SUSCEPTIBILITY TO, 5; DYX5
MIM:608995 - DYSLEXIA, SUSCEPTIBILITY TO, 8; DYX8

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

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