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DOID:14177 - congenital hypogammaglobulinemia
Disease Ontology Definition:n_a
Synonyms: Congenital hypogammaglobulinemia (finding), Congenital hypogammaglobulinemia, Congenital hypogammaglobulinaemia
Xenbase Genes
| MONDO:0001902 - epithelium of small intestine |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s):
B cell deficiency (is_a),
physical disorder (is_a)
