Recurrent infection of the gastrointestinal tract

Symptom Information:

Symptom ID: HPO:0004798
Synonyms:
Gastrointestinal infections [HPO:0004798]
GASTROINTESTINAL INFECTIONS, RECURRENT [HPO:0004798]
Recurrent gastrointestinal infections [HPO:0004798]
Gastrointestinal infections [OMIM:Gastrointestinal infections]
Gastrointestinal infections, recurrent [OMIM:Gastrointestinal infections, recurrent]
Recurrent gastrointestinal infections [OMIM:Recurrent gastrointestinal infections]
Recurrent gastrointestinal infections (1 patient) [OMIM:Recurrent gastrointestinal infections (1 patient)]
Gastrointestinal infections [MedDRA:10017966]
Gastrointestinal infection [MedDRA:10017964]
Quality:
Cross references:
OMIM: "Gastrointestinal infections" [OMIM:Gastrointestinal infections]
OMIM: "Gastrointestinal infections, recurrent" [OMIM:Gastrointestinal infections, recurrent]
OMIM: "Recurrent gastrointestinal infections" [OMIM:Recurrent gastrointestinal infections]
OMIM: "Recurrent gastrointestinal infections (1 patient)" [OMIM:Recurrent gastrointestinal infections (1 patient)]
Is a (Direct Parents):
MedDRA Gastrointestinal infections, site unspecified
HPO         Abnormality of the gastrointestinal tract
MedDRA Gastrointestinal disorders
HPO         Recurrent infections
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
             Recurrent infections(HPO:0002719)
                Recurrent infection of the gastrointestinal tract(HPO:0004798)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the gastrointestinal tract(HPO:0011024)
                Recurrent infection of the gastrointestinal tract(HPO:0004798)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Recurrent infection of the gastrointestinal tract(HPO:0004798)
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

COG4-CDG (Orphanet:263501)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMALDOMINANT (OMIM:612132)
Hyper-IgM syndrome type 2 (Orphanet:101089)
Hyper-IgM syndrome type 4 (Orphanet:101091)
IMMUNOGLOBULIN A DEFICIENCY 1 (OMIM:137100)
IMMUNOGLOBULIN A DEFICIENCY 2 (OMIM:609529)
Nijmegen breakage syndrome (Orphanet:647)
X-linked reticulate pigmentary disorder with systemic manifestations (Orphanet:85453)