Disease #01918 (HMAG (methylcobalamin deficiency, cblG type (HMAG)), OMIM:250940)

Official abbreviation HMAG
Name methylcobalamin deficiency, cblG type (HMAG)
OMIM ID 250940
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MTR
Associated tissues -
Disease features -
Remarks -