decreased adenosylcobalamin Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Decreased concentration of adenosylcobalamin. Adenosylcobalamin is one of the active forms of vitamin B12. (Human Phenotype Ontology, HP_0003145)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003145
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Genes

6 genes associated with the decreased adenosylcobalamin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCD4 ATP-binding cassette, sub-family D (ALD), member 4
LMBRD1 LMBR1 domain containing 1
MMAA methylmalonic aciduria (cobalamin deficiency) cblA type
MMAB methylmalonic aciduria (cobalamin deficiency) cblB type
MMACHC methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
MMADHC methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria