Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to [Supplementary Concept]

mutation in UMPH1

Date introduced: November 5, 2012

MeSH Unique ID: C564859

Heading Mapped to:

• Anemia, Hemolytic, Congenital
• 5'-Nucleotidase/deficiency

Entry Terms:

• UMPH1 Deficiency
• Pyrimidine 5-Prime Nucleotidase Deficiency, Hemolytic Anemia due to
• Hemolytic Anemia due to UMPH1 Deficiency
• Hemolytic Anemia due to P5N Deficiency
• Hemolytic Anemia due to Uridine 5-Prime Monophosphate Hydrolase Deficiency