- OMIM ID
-
236270
- OMIM term:
- HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA DUE TO DEFECT IN COBALAMIN METABOLISM, cblE COMPLEMENTATION TYPE
- Alternative terms:
-
VITAMIN B12-RESPONSIVE HOMOCYSTINURIA, cblE TYPE
METHYLCOBALAMIN DEFICIENCY, cblE TYPE
- (∗) Location:
- 5p15.31
- (†) Associated OMIM genes:
- MTRR
- (‡) Associated MGI genes:
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