DYSLEXIA, SUSCEPTIBILITY TO, 8

General Information (adopted from Orphanet):

Synonyms, Signs: DYX8
Number of Symptoms 6
OrphanetNr:
OMIM Id: 608995
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant inheritance
Multifactorial
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0010522) Dyslexia 7 / 7739
2
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739
3
(HPO:0001426) Multifactorial inheritance 37 / 7739
4
(OMIM) Difficulty in phonologic coding 1 / 7739
5
(OMIM) Difficulty in spelling 1 / 7739
6
(OMIM) Decreased rapid automatized naming (RAN) speed 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: