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combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia

Disease Summary
Associated Targets (1)
Tchem

1


Uniprot Description An autosomal recessive disorder due to an inborn error of folate metabolism. Variable clinical manifestations include hemolytic uremic syndrome, macrocytosis, epilepsy, hearing loss, retinopathy, mild mental retardation, and lymphopenia.
Mondo Term and Equivalent IDs
MONDO:0060611:  combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia
UMLS:C4540434: