MeSH Browser

MeSH Supplementary: Methylmalonic Aciduria and Homocystinuria, CblF Type
Unique ID: C564747
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564747
Entry Term(s): Cobalamin F Disease; Cobalamin, Defect in Lysosomal Release of; Methylmalonic Acidemia and Homocystinuria, CblF Type; Methylmalonic Aciduria due to Vitamin B12-Release Defect; Vitamin B12 Lysosomal Release Defect; Vitamin B12 Storage Disease
Registry Number: 0
Heading Mapped to: *Amino Acid Metabolism, Inborn Errors
Frequency: 9
Note: mutation in LMBRD1
Date of Entry: 2012/11/05

Methylmalonic Aciduria and Homocystinuria, CblF Type MeSH Supplementary Concept Data 2024