Preferred Name |
Neonatal hemochromatosis |
|
Synonyms |
Neonatal hepatitis |
|
ID |
http://purl.bioontology.org/ontology/MESH/C536394 |
|
altLabel |
Neonatal hepatitis Giant cell hepatitis Hemochromatosis, Neonatal Idiopathic Neonatal Hemochromatosis PIGCH post infantile giant cell hepatitis Alloimmune Hepatitis, Congenital |
|
cui |
C5200297 C0268059 C0027613 |
|
HM |
D006432 |
|
Inverse of RB |
0 |
|
Mapped to | ||
MDA |
20100825 |
|
MeSH Frequency |
79 |
|
MMR |
20191030 |
|
notation |
C536394 |
|
prefLabel |
Neonatal hemochromatosis |
|
SC |
3 |
|
Scope Statement |
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 |
|
TERMUI |
T739196 T000961461 T000961643 T827124 T800969 T000961462 T739195 |
|
TH |
OMIM (2013) NLM (2019) ORD (2010) |
|
tui |
T047 |
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