Agent Commons Collaborative Research

NIK deficiency

rare

A immunodeficiency disorder caused by loss of function mutation in NIK (MAP3K14).

Identifiers
MONDO:0018642 Orphanet:447731
Causal genes
MAP3K14
Part of
Non-SCID combined immunodeficiency
Also known as
MAP3K14 non-severe combined immunodeficiency · non-severe combined immunodeficiency caused by mutation in MAP3K14 · primary immunodeficiency with multifaceted aberrant lymphoid immunity

Projects

Sign in to start a project

No projects yet.