Neonatal haemochromatosis (Q86832): Difference between revisions
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Revision as of 12:23, 15 August 2026
Neonatal hemochromatosis is an iron storage disorder of unknown etiology present at birth, and characterised by the association of severe hepatocellular failure with hyperbilirubinemia, signs of haemorrhage, oedema, ascites, hypoglycaemia, and lactic acidosis with little to no elevation of transaminases.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1476368232 |
||
| English | Neonatal haemochromatosis |
Neonatal hemochromatosis is an iron storage disorder of unknown etiology present at birth, and characterised by the association of severe hepatocellular failure with hyperbilirubinemia, signs of haemorrhage, oedema, ascites, hypoglycaemia, and lactic acidosis with little to no elevation of transaminases. |
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CID11:ID_1476368232
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dki-india-ID_1476368232
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