5.1.3.14	Amyloidosis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16121806&form=6&db=m	Peripheral genotype-phenotype correlations in Asian Indians with type 2 diabetes mellitus.	causal interaction,unassigned	1,0	
5.1.3.14	Anemia	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16121806&form=6&db=m	Peripheral genotype-phenotype correlations in Asian Indians with type 2 diabetes mellitus.	causal interaction,unassigned	1,0	
5.1.3.14	Bardet-Biedl Syndrome	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16121806&form=6&db=m	Peripheral genotype-phenotype correlations in Asian Indians with type 2 diabetes mellitus.	causal interaction,unassigned	1,0	
5.1.3.14	Breast Neoplasms	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16121806&form=6&db=m	Peripheral genotype-phenotype correlations in Asian Indians with type 2 diabetes mellitus.	causal interaction,unassigned	1,0	
5.1.3.14	Carcinoma	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16121806&form=6&db=m	Peripheral genotype-phenotype correlations in Asian Indians with type 2 diabetes mellitus.	causal interaction,unassigned	1,0	
5.1.3.14	Carcinoma	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=22049060&form=6&db=m	Loss of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) induces apoptotic processes in pancreatic carcinoma cells.	causal interaction,diagnostic usage,ongoing research,unassigned	2,3,4,0	
5.1.3.14	Carcinoma, Hepatocellular	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7414604&form=6&db=m	UDP-N-acetylglucosamine 2'-epimerase of rat hepatoma and its comparison with the enzyme of rat liver.	ongoing research,unassigned	4,0	
5.1.3.14	Distal Myopathies	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11916006&form=6&db=m	Nonaka myopathy is caused by mutations in the UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase gene (GNE).	causal interaction,unassigned	3,0	
5.1.3.14	Distal Myopathies	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12177386&form=6&db=m	Distal myopathy with rimmed vacuoles: novel mutations in the GNE gene.	causal interaction,unassigned	3,0	
5.1.3.14	Distal Myopathies	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=14678807&form=6&db=m	A novel homozygous missense mutation in the GNE gene of a patient with quadriceps-sparing hereditary inclusion body myopathy associated with muscle inflammation.	causal interaction,unassigned	1,0