CHROMOSOME Xp22 DELETION SYNDROME

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 7
OrphanetNr:
OMIM Id: 300830
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:0001249) Intellectual disability 1089 / 7739
2
 (HPO:0007018) Attention deficit hyperactivity disorder 56 / 7739
3
 (HPO:0100710) Impulsivity 16 / 7739
4
 (HPO:0000729) Autistic behavior obligate [HPO:skoehler] 27 / 7739
5
 (HPO:0000718) Aggressive behavior 109 / 7739
6
 (HPO:0100034) Motor tics 5 / 7739
7
 (HPO:0001252) Muscular hypotonia rare [HPO:skoehler] 990 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: