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dyslexia
Summary
- Definition
- A reading disorder resulting from a developmental reading disability involving the inability to process graphic symbols resulting in impairment of reading ability.
- Super Class
- reading disorder
External Links
- Disease Ontology
- DOID:4428
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 142 | PARP1 | poly(ADP-ribose) polymerase 1 | |
| 414 | ARSD | arylsulfatase D | |
| 1312 | COMT | catechol-O-methyltransferase | |
| 1463 | NCAN | neurocan | |
| 1588 | CYP19A1 | cytochrome P450 family 19 subfamily A member 1 | |
| 1738 | DLD | dihydrolipoamide dehydrogenase | |
| 7957 | EPM2A | EPM2A glucan phosphatase, laforin | |
| 8398 | PLA2G6 | phospholipase A2 group VI | |
| 9162 | DGKI | diacylglycerol kinase iota | |
| 10728 | PTGES3 | prostaglandin E synthase 3 |
Related Glycoprotein
