2.5.1.151	alkylcobalamin dealkylase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=32186706&form=6&db=m	The vitamin B12 processing enzyme, mmachc, is essential for zebrafish survival, growth and retinal morphology.	causal interaction,therapeutic application,unassigned	4,1,0	
2.5.1.151	alkylcobalamin dealkylase deficiency	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34147638&form=6&db=m	Absence of MMACHC in peripheral retinal cells does not lead to an ocular phenotype in mice.	causal interaction,therapeutic application,unassigned	3,1,0	
2.5.1.151	Anemia, Megaloblastic	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23825108&form=6&db=m	Interaction between methionine synthase isoforms and MMACHC: characterization in cblG-variant, cblG and cblC inherited causes of megaloblastic anaemia.	unassigned	-	
2.5.1.151	Avitaminosis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31905202&form=6&db=m	THAP11F80L cobalamin disorder-associated mutation reveals normal and pathogenic THAP11 functions in gene expression and cell proliferation.	causal interaction,unassigned	3,0	
2.5.1.151	Craniofacial Abnormalities	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25281006&form=6&db=m	Hcfc1b, a zebrafish ortholog of HCFC1, regulates craniofacial development by modulating mmachc expression.	unassigned	-	
2.5.1.151	Genetic Diseases, Inborn	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26464686&form=6&db=m	Genetic analysis of four cases of methylmalonic aciduria and homocystinuria, cblC type#.	diagnostic usage,therapeutic application,unassigned	3,1,0	
2.5.1.151	Glycogen Storage Disease Type VI	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24974159&form=6&db=m	First Chinese case of successful pregnancy with combined methylmalonic aciduria and homocystinuria, cblC type.	causal interaction,diagnostic usage,ongoing research,unassigned	1,4,1,0	
2.5.1.151	Homocystinuria	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18164228&form=6&db=m	Spectrum of MMACHC mutations in Italian and Portuguese patients with combined methylmalonic aciduria and homocystinuria, cblC type.	therapeutic application,unassigned	1,0	
2.5.1.151	Homocystinuria	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18848477&form=6&db=m	Ocular phenotype in patients with methylmalonic aciduria and homocystinuria, cobalamin C type.	ongoing research,unassigned	2,0	
2.5.1.151	Homocystinuria	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19370762&form=6&db=m	Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlations.	causal interaction,unassigned	3,0