Bare lymphocyte syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
BARE LYMPHOCYTE SYNDROME
C0242583
CIITA Unknown — Disgenet
BARE LYMPHOCYTE SYNDROME 2
C2931418MESH:C537079
CIITA Unknown — CTD, Disgenet
RFX5 Unknown — Disgenet
RFXANK Unknown — Disgenet
RFXAP Unknown — Disgenet
BARE LYMPHOCYTE SYNDROME, TYPE I
C1858266MESH:C565759
B2M Unknown — Disgenet
TAP1 Unknown
10074494
CTD, Disgenet
TAP2 Unknown — Disgenet
TAPBP Unknown — Disgenet
BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP A
C1859534
CIITA Unknown — Disgenet
RFX5 Unknown — Disgenet
RFXANK Unknown — Disgenet
All8 Causal0 Unknown8
Related Diseases Diseases that share the most curated genes with Bare lymphocyte syndrome.
5 View disease cluster →
MHC class II deficiency 4 shared genesCIITA, RFX5, RFXANK, RFXAP Related via 4 shared genes including CIITA, RFX5, RFXANK. MHC class I deficiency 3 shared genesTAP2, TAP1, TAPBP Related via 3 shared genes including TAP2, TAP1, TAPBP. Beta2-microglobulinic amyloidosis 1 shared geneB2M Related via 1 shared gene including B2M. Hypergammaglobulinemia 1 shared geneB2M Related via 1 shared gene including B2M. amyloidosis, hereditary systemic 6 1 shared geneB2M Related via 1 shared gene including B2M.