reticular dysgenesis Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A severe combined immunodeficiency that is the most severe form of SCID and is caused by mutations in the gene encoding mitochondrial adenylate kinase 2. It is characterized by congenital agranulocytosis, lymphopenia, and lymphoid and thymic hypoplasia with absent cellular and humoral immunity functions. (Human Disease Ontology, DOID_0060020)
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17 genes co-occuring with the disease reticular dysgenesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
AK2 adenylate kinase 2 2.54568
AK7 adenylate kinase 7 1.50974
GFI1B growth factor independent 1B transcription repressor 1.3027
AK1 adenylate kinase 1 1.0585
NME4 NME/NM23 nucleoside diphosphate kinase 4 0.993596
GFI1 growth factor independent 1 transcription repressor 0.97338
AGPS alkylglycerone phosphate synthase 0.951604
CKMT2 creatine kinase, mitochondrial 2 (sarcomeric) 0.94369
IL2RG interleukin 2 receptor, gamma 0.833968
ADA adenosine deaminase 0.712392
JAK3 Janus kinase 3 0.668345
XBP1 X-box binding protein 1 0.608885
AIRE autoimmune regulator 0.503441
IL2 interleukin 2 0.330295
CD40LG CD40 ligand 0.275801
CD5 CD5 molecule 0.216332
FOXP3 forkhead box P3 0.172038