abnormality of the peritoneum Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the peritoneum. (Human Phenotype Ontology, HP_0002585)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002585
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Genes

17 genes associated with the abnormality of the peritoneum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BCL2 B-cell CLL/lymphoma 2
BCL6 B-cell CLL/lymphoma 6
BRCA1 breast cancer 1, early onset
COL1A1 collagen, type I, alpha 1
COL5A1 collagen, type V, alpha 1
COL5A2 collagen, type V, alpha 2
EWSR1 EWS RNA-binding protein 1
F5 coagulation factor V (proaccelerin, labile factor)
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
JAK2 Janus kinase 2
MEFV Mediterranean fever
MVK mevalonate kinase
SLC29A3 solute carrier family 29 (equilibrative nucleoside transporter), member 3
SOX18 SRY (sex determining region Y)-box 18
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A
WT1 Wilms tumor 1