Chylothorax Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Accumulation of excessive amounts of lymphatic fluid (chyle) in the pleural cavity. (Human Phenotype Ontology, HP_0010310)
External Link https://www.disgenet.org/browser/0/1/0/C0008733
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Genes

23 genes associated with the disease Chylothorax in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACR acrosin
ADAMTS3 ADAM metallopeptidase with thrombospondin type 1 motif, 3
ADIPOQ adiponectin, C1Q and collagen domain containing
BTNL2 butyrophilin-like 2
CCBE1 collagen and calcium binding EGF domains 1
CFD complement factor D (adipsin)
FAT4 FAT atypical cadherin 4
FLT4 fms-related tyrosine kinase 4
FOXC2 forkhead box C2
GDF1 growth differentiation factor 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
ITGA9 integrin, alpha 9
KIF11 kinesin family member 11
MAP4K4 mitogen-activated protein kinase kinase kinase kinase 4
PPP1R13L protein phosphatase 1, regulatory subunit 13 like
RASA1 RAS p21 protein activator (GTPase activating protein) 1
RIT1 Ras-like without CAAX 1
RNH1 ribonuclease/angiogenin inhibitor 1
SHC3 SHC (Src homology 2 domain containing) transforming protein 3
SOX18 SRY (sex determining region Y)-box 18
SST somatostatin
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2