AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 10
OrphanetNr:
OMIM Id: 616100
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:0002788) Recurrent upper respiratory tract infections rare [HPO:skoehler] 31 / 7739
2
 (HPO:0001744) Splenomegaly 337 / 7739
3
 (HPO:0002240) Hepatomegaly 467 / 7739
4
 (HPO:0002014) Diarrhea 225 / 7739
5
 (HPO:0003765) Psoriasis rare [HPO:skoehler] 17 / 7739
6
 (HPO:0000964) Eczema rare [HPO:skoehler] 81 / 7739
7
 (HPO:0001890) Autoimmune hemolytic anemia 17 / 7739
8
 (HPO:0004313) Decreased antibody level in blood 47 / 7739
9
 (HPO:0001973) Autoimmune thrombocytopenia 18 / 7739
10
 (HPO:0002716) Lymphadenopathy 129 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: