MeSH Browser

MeSH Supplementary: Neonatal hemochromatosis
Unique ID: C536394
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536394
Entry Term(s): Alloimmune Hepatitis, Congenital; Giant cell hepatitis; Hemochromatosis, Neonatal; Idiopathic Neonatal Hemochromatosis; Neonatal hepatitis; PIGCH post infantile giant cell hepatitis
Registry Number: 0
Heading Mapped to: *Hemochromatosis
Frequency: 79
Note: A hereditary autosomal recessive disorder characterized by LIVER FAILURE in the neonatal period and heavy iron staining in the liver. There are also iron deposits in extrahepatic tissues, including the heart and pancreas. OMIM: 231100
Date of Entry: 2010/08/25
Revision Date: 2019/10/30

Neonatal hemochromatosis MeSH Supplementary Concept Data 2024