| Human Disease |
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due to OMIM ID: 266120 |
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| Synonyms | Hemolytic Anemia Due to P5n Deficiency; Hemolytic Anemia Due to Umph1 Deficiency; P5N Deficiency; Pyrimidine 5-Prime Nucleotidase Deficiency, Hemolytic Anemia Due to; UMPH1 Deficiency | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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