Gene: CA5A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 763
Gene Symbol: CA5A
CA5A 		0.110 Biomarker phenotype BEFREE CA-VA deficiency should therefore be added to urea cycle defects, organic acidurias, and pyruvate carboxylase deficiency as a treatable condition in the differential diagnosis of hyperammonemia in the neonate and young child. 24530203 2014
Entrez Id: 763
Gene Symbol: CA5A
CA5A 		0.110 Biomarker phenotype HPO