Transient hypogammaglobulinemia of infancy

Symptom Information:

Symptom ID: HPO:0005432
Synonyms:
Newborn gammaglobulin deficiency [HPO:0005432]
Newborn gammaglobulin deficiency [OMIM:Newborn gammaglobulin deficiency]
Quality:
Cross references:
OMIM: "Newborn gammaglobulin deficiency" [OMIM:Newborn gammaglobulin deficiency]
Is a (Direct Parents):
HPO         Decreased antibody level in blood
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)
             Abnormality of humoral immunity(HPO:0005368)
                Abnormal immunoglobulin level(HPO:0010701)
                   Decreased antibody level in blood(HPO:0004313)
                      Transient hypogammaglobulinemia of infancy(HPO:0005432)
          Abnormality of cellular immune system(HPO:0010987)
             Abnormality of leukocytes(HPO:0001881)
                Abnormality of lymphocytes(HPO:0004332)
                   Abnormality of B cells(HPO:0002846)
                      Abnormality of B cell physiology(HPO:0005372)
                         Abnormal immunoglobulin level(HPO:0010701)
                            Decreased antibody level in blood(HPO:0004313)
                               Transient hypogammaglobulinemia of infancy(HPO:0005432)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of leukocytes(HPO:0001881)
             Abnormality of lymphocytes(HPO:0004332)
                Abnormality of B cells(HPO:0002846)
                   Abnormality of B cell physiology(HPO:0005372)
                      Abnormal immunoglobulin level(HPO:0010701)
                         Decreased antibody level in blood(HPO:0004313)
                            Transient hypogammaglobulinemia of infancy(HPO:0005432)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Say-Barber-Miller syndrome (Orphanet:3132)