IMMUNODEFICIENCY, COMMON VARIABLE, 10

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 10
OrphanetNr:
OMIM Id: 615577
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:0001263) Global developmental delay rare [HPO:skoehler] 853 / 7739
2
 (HPO:0011734) Central adrenal insufficiency 2 / 7739
3
 (HPO:0000824) Growth hormone deficiency rare [HPO:skoehler] 56 / 7739
4
 (HPO:0008404) Nail dystrophy rare [HPO:skoehler] 89 / 7739
5
 (HPO:0001596) Alopecia rare [HPO:skoehler] 162 / 7739
6
 (HPO:0004313) Decreased antibody level in blood 47 / 7739
7
 (HPO:0002205) Recurrent respiratory infections 254 / 7739
8
 (HPO:0002099) Asthma 62 / 7739
9
 (HPO:0002721) Immunodeficiency 97 / 7739
10
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: