MeSH Browser

MeSH Supplementary: NADH cytochrome B5 reductase deficiency
Unique ID: C537841
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537841
Entry Term(s): Diaphorase deficiency; Methemoglobinemia due to deficiency of methemoglobin reductase; Methemoglobinemia, Congenital, Autosomal Recessive; Methemoglobinemia, Type I; Methemoglobinemia, Type Ii; NADH diaphorase deficiency; NADH methemoglobin reductase deficiency; NADH-dependent methemoglobin reductase deficiency; Nadh-Cytochrome B5 Reductase Deficiency; Nadh-Cytochrome B5 Reductase Deficiency, Type I; Nadh-Cytochrome B5 Reductase Deficiency, Type Ii
Registry Numbers: 0
Heading Mapped to: *Methemoglobinemia; Cytochrome-B(5) Reductase / deficiency
Frequency: 13
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

NADH cytochrome B5 reductase deficiency MeSH Supplementary Concept Data 2025