lymphoid interstitial pneumonia Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An idiopathic interstitial pneumonia which involves diffuse interstitial infiltration of involved areas mostly with T lymphocytes, plasma cells, and macrophages. Lymphoid hyperplasia is frequently seen. Onset is often slow with gradually increasing cough and breathlessness over 3 or more years. Fever, weight loss, chest pain, and arthralgia are occasionally found. Crackles may be detected as the disease progresses. (Human Disease Ontology, DOID_0050159)
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17 genes co-occuring with the disease lymphoid interstitial pneumonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
TPPP tubulin polymerization promoting protein 1.09839
FIGF c-fos induced growth factor (vascular endothelial growth factor D) 0.901156
NDN necdin, melanoma antigen (MAGE) family member 0.844621
CD4 CD4 molecule 0.738271
FLCN folliculin 0.698715
LIG3 ligase III, DNA, ATP-dependent 0.595623
TRIM21 tripartite motif containing 21 0.571107
HSPG2 heparan sulfate proteoglycan 2 0.562558
SH2D1A SH2 domain containing 1A 0.551686
TGFB1 transforming growth factor, beta 1 0.47374
MNX1 motor neuron and pancreas homeobox 1 0.451454
HLA-C major histocompatibility complex, class I, C 0.398216
SELL selectin L 0.396725
BCL6 B-cell CLL/lymphoma 6 0.350452
CD79A CD79a molecule, immunoglobulin-associated alpha 0.332852
IL6 interleukin 6 0.197742
CD5 CD5 molecule 0.162707