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DOID:14177 - congenital hypogammaglobulinemia
Disease Ontology Definition:n_a
Synonyms: Congenital hypogammaglobulinaemia, Congenital hypogammaglobulinemia, Congenital hypogammaglobulinemia (finding),
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0001902 - congenital agammaglobulinemia |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
B cell deficiency (is_a),
physical disorder (is_a)