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L-ferritin deficiency, autosomal recessive

MedGen UID:
864488
Concept ID:
C4016051
Finding
Synonym: L-FERRITIN DEFICIENCY, AUTOSOMAL RECESSIVE
 
OMIM®: 134790

Recent clinical studies

Diagnosis

Ponka P
Ann N Y Acad Sci 2004 Mar;1012:267-81. doi: 10.1196/annals.1306.022. PMID: 15105272

Prognosis

Ponka P
Ann N Y Acad Sci 2004 Mar;1012:267-81. doi: 10.1196/annals.1306.022. PMID: 15105272
Ponka P
Semin Hematol 2002 Oct;39(4):249-62. doi: 10.1053/shem.2002.35638. PMID: 12382200

Clinical prediction guides

Ponka P
Ann N Y Acad Sci 2004 Mar;1012:267-81. doi: 10.1196/annals.1306.022. PMID: 15105272
Ponka P
Semin Hematol 2002 Oct;39(4):249-62. doi: 10.1053/shem.2002.35638. PMID: 12382200

Supplemental Content

Table of contents

    Clinical resources

    Consumer resources