MENTAL RETARDATION, X-LINKED 101

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 9
OrphanetNr:
OMIM Id: 300928
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0000276) Long face rare [HPO:skoehler] 109 / 7739
2
 (HPO:0000486) Strabismus 576 / 7739
3
 (HPO:0000400) Macrotia rare [HPO:skoehler] 108 / 7739
4
 (HPO:0002465) Poor speech 31 / 7739
5
 (HPO:0001263) Global developmental delay 853 / 7739
6
 (HPO:0001249) Intellectual disability 1089 / 7739
7
 (HPO:0001344) Absent speech 57 / 7739
8
 (HPO:0000752) Hyperactivity 140 / 7739
9
 (HPO:0001250) Seizures rare [HPO:skoehler] 1245 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: