Human Phenotype Ontology 
Grandparent Node:
expandAbnormal immunoglobulin level (HP:0010701)help
Parent Node:
expandDecreased circulating antibody level (HP:0004313)help
..Starting node
..expandTransient hypogammaglobulinemia of infancy (HP:0005432)help
Term ID: 5432
Name: Transient hypogammaglobulinemia of infancy
Synonym: Newborn gammaglobulin deficiency
Definition: At birth, newborns are endowed with maternal antibodies. IgG production normally begins at the age of two months. A delay in recovery from this physiological hypogammaglobulinemia between the 3rd and the 6th month of life, and of recovery period between 18 and 36 months defines transient newborn hypogammaglobulinemia.
Comments:
Reference: HP:0005432
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAgammaglobulinemia (HP:0004432) help
..expandDecreased circulating IgA level (HP:0002720) help
..expandDecreased circulating IgE (HP:0005479) help
..expandDecreased circulating IgG level (HP:0004315) help
..expandDecreased circulating total IgM (HP:0002850) help
..expandDysgammaglobulinemia (HP:0002961) help
..expandPanhypogammaglobulinemia (HP:0003139) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005432HP:0005432Transient hypogammaglobulinemia of infancy0 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.