2.1.1.228	Nervous System Diseases	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30415557&form=6&db=m	tRNA Methyltransferase Defects and Intellectual Disability.	diagnostic usage,ongoing research,therapeutic application,unassigned	2,1,1,0	
2.1.1.228	Microcephaly	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24204302&form=6&db=m	tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans.	causal interaction,ongoing research,therapeutic application,unassigned	4,1,1,0	
2.1.1.228	Diabetes Mellitus	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26526202&form=6&db=m	tRNA methyltransferase homologue gene TRMT10A mutation in young adult-onset diabetes with intellectual disability, microcephaly and epilepsy.	causal interaction,ongoing research,therapeutic application,unassigned	4,1,3,0	
2.1.1.228	Epilepsy	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26526202&form=6&db=m	tRNA methyltransferase homologue gene TRMT10A mutation in young adult-onset diabetes with intellectual disability, microcephaly and epilepsy.	causal interaction,ongoing research,therapeutic application,unassigned	4,1,3,0	
2.1.1.228	Intellectual Disability	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26526202&form=6&db=m	tRNA methyltransferase homologue gene TRMT10A mutation in young adult-onset diabetes with intellectual disability, microcephaly and epilepsy.	causal interaction,ongoing research,therapeutic application,unassigned	4,1,3,0	
2.1.1.228	Microcephaly	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26526202&form=6&db=m	tRNA methyltransferase homologue gene TRMT10A mutation in young adult-onset diabetes with intellectual disability, microcephaly and epilepsy.	causal interaction,ongoing research,therapeutic application,unassigned	4,1,3,0