MeSH Browser

MeSH Supplementary: Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to
Unique ID: C564859
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564859
Entry Term(s): Hemolytic Anemia due to P5N Deficiency; Hemolytic Anemia due to UMPH1 Deficiency; Hemolytic Anemia due to Uridine 5-Prime Monophosphate Hydrolase Deficiency; Pyrimidine 5-Prime Nucleotidase Deficiency, Hemolytic Anemia due to; UMPH1 Deficiency
Registry Numbers: 0
Heading Mapped to: *Anemia, Hemolytic, Congenital; 5'-Nucleotidase / deficiency
Frequency: 4
Note: mutation in UMPH1
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to MeSH Supplementary Concept Data 2025