NFKB2, nuclear factor kappa B subunit 2, 4791

N. diseases: 194; N. variants: 12
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0263504
Disease: Alopecia totalis
Alopecia totalis
0.110 GeneticVariation disease BEFREE We report a pediatric patient who initially presented with hypogammaglobulinemia and alopecia totalis, who was identified to have a de novo NFKB2 mutation at one year of age. 31150062 2019
CUI: C0263504
Disease: Alopecia totalis
Alopecia totalis
0.110 Biomarker disease HPO