MeSH Browser

MeSH Supplementary: Combined Oxidative Phosphorylation Deficiency 2
Unique ID: C566468
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566468
Entry Term(s): COXPD2; Corpus Callosum, Agenesis Of, With Dysmorphism And Fatal Lactic Acidosis
Registry Number: 0
Heading Mapped to: *Acidosis, Lactic; *Craniofacial Abnormalities; *Agenesis of Corpus Callosum
Frequency: 0
Date of Entry: 2012/11/05

Combined Oxidative Phosphorylation Deficiency 2 MeSH Supplementary Concept Data 2024