Disease #02782 (AICAR transformylase/IMP cyclohydrolase deficiency, OMIM:608688)

Official abbreviation -
Name AICAR transformylase/IMP cyclohydrolase deficiency
OMIM ID 608688
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ATIC
Associated tissues -
Disease features -
Remarks -