MeSH Browser

MeSH Supplementary: AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency
Unique ID: C563876
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563876
Entry Term(s): AICA Ribosuria due to ATIC Deficiency
Registry Numbers: 0
Heading Mapped to: *Congenital Abnormalities; *Epilepsy; *Intellectual Disability; Nucleotide Deaminases / deficiency; Hydroxymethyl and Formyl Transferases / deficiency
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency MeSH Supplementary Concept Data 2025