About: neonatal hemochromatosis

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

medical condition

Attributes	Values
rdf:type	Item
description	medical condition (en) Krankheit (de) malattia (it) медичний стан (uk)
exact match	wds:Q1627324-B41E46E4-F9F6-4C8D-B0AB-6D6CA68AFD6A
exact match	http://www.orpha.net/ORDO/Orphanet_446
Mondo ID	wds:Q1627324-BB8CA385-7EFA-4289-AF22-6C3A693EDC2F
DiseasesDB	wds:Q1627324-8CF90658-A093-44F4-9AD8-186FAE1E17C5
Mondo ID	http://purl.obolibrary.org/obo/MONDO_0009275
Mondo ID	MONDO_0009275
DiseasesDB	34508
rdfs:label	Neonatale Hämochromatose (de) hémochromatose néonatale (fr) neonatal hemochromatosis (en)
skos:prefLabel	Neonatale Hämochromatose (de) hémochromatose néonatale (fr) neonatal hemochromatosis (en)
name	Neonatale Hämochromatose (de) hémochromatose néonatale (fr) neonatal hemochromatosis (en)
instance of	wds:Q1627324-D6F2E165-6707-423C-A811-B0EC347EBF29
instance of	class of disease
subclass of	wds:Q1627324-4F810C7D-6D4A-40E9-A927-FD144ACC5EE0
subclass of	iron overload
Orphanet ID	wds:Q1627324-A33D423D-0205-4EFB-9D98-62ECBB357430 wds:Q1627324-AF996A99-5E29-4872-9A6B-2F9FCCDD5CDB
ICD-10-CM	wds:Q1627324-CF362CF8-E83D-421B-A901-0E822E87BC62
GARD rare disease ID	wds:Q1627324-CD05E42A-FD5E-45B1-BD12-15134E28003A
OMIM ID	wds:Q1627324-969ABDE5-AC1F-49A3-8786-8CF464F23B47
Orphanet ID	446
ICD-10-CM	E83.1
GARD rare disease ID	7172
OMIM ID	231100
skos:altLabel	Nh (en) Alloimmune Hepatitis, Congenital (en) Giant Cell Hepatitis (en) Giant Cell Hepatitis (formerly) (en) Giant Cell Hepatitis, Formerly (en) HEMOCHROMATOSIS, NEONATAL (en) Hemochromatosis neonatal (en) Idiopathic neonatal Hemochromatosis (en) Neonatal Hepatitis (en) Neonatal Hepatitis, Formerly (en) Neonatal hepatitis (formerly) (en) Nhc (en)
NCI Thesaurus ID	wds:Q1627324-77102EEE-9D19-496D-809C-38BEB1A595B7 wds:Q1627324-EB647AA3-2621-4BBA-94AA-852EA2D255CE
UMLS CUI	wds:Q1627324-226CC45F-ECA6-48FC-A128-F8152D9C61B5 wds:Q1627324-76ECCAB7-D23D-470B-9BDB-F246D63605B2
MeSH descriptor ID	wds:Q1627324-5A480392-24C9-4BC8-A8ED-CBADF647B825 wds:Q1627324-6EBBB486-C953-48B5-BB45-397A5AA4BB56
Microsoft Academic ID	wds:Q1627324-19A708B9-FA55-42A1-A7DE-58D23A1370F0 wds:Q1627324-43BC2050-7776-4577-970D-195668FD16D3
ICD-11 (foundation)	wds:Q1627324-DAE792DA-5679-4F87-87FF-84B8A0865850
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/C536394
Microsoft Academic ID	https://makg.org/entity/2780240347 https://makg.org/entity/2909017162
NCI Thesaurus ID	C129980
UMLS CUI	C0027613 C0268059
MeSH descriptor ID	C536394
Microsoft Academic ID	2780240347 2909017162
ICD-11 (foundation)	1476368232
WikiProjectMed ID	wds:Q1627324-F6F5D360-39FB-4703-8FA1-1AA154FB17E1
WikiProjectMed ID	Neonatal hemochromatosis
is owl:sameAs of	neonatal hemochromatosis
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q1627324 Neonatal hemochromatosis https://de.wikipedia.org/wiki/Neonatale_H%C3%A4mochromatose
is main subject of	Studies in neonatal hepatitis and biliary atresia. IV. Diagnosis Patent ductus venosus and acute liver failure in the neonate: consider neonatal hemochromatosis with liver scarring Probable intrafamilial transmission of coxsackievirus b3 with vertical transmission, severe early-onset neonatal hepatitis, and prolonged viral RNA shedding Safety of neonatal hepatitis B vaccine administration Significance and anamnestic response in isolated hepatitis B core antibody-positive individuals 18 years after neonatal hepatitis B virus vaccination in Taiwan Neonatal hemochromatosis: outcomes of pharmacologic and surgical therapies Oropharyngeal and upper respiratory tract mucosal-gland siderosis in neonatal hemochromatosis: an approach to biopsy diagnosis. Prenatal diagnosis of idiopathic neonatal hemochromatosis with MRI Liver transplantation in newborn liver failure: treatment for neonatal hemochromatosis Outcome of pregnancies at risk for neonatal hemochromatosis is improved by treatment with high-dose intravenous immunoglobulin. Studies of the aetiology of neonatal hepatitis and biliary atresia Familial giant cell hepatitis associated with synthesis of 3 beta, 7 alpha-dihydroxy-and 3 beta,7 alpha, 12 alpha-trihydroxy-5-cholenoic acids Considerations of the pathogenesis of neonatal hepatitis, biliary atresia and choledochal cyst--the concept of infantile obstructive cholangiopathy Cytomegalovirus and human herpesvirus 6, but not human papillomavirus, are present in neonatal giant cell hepatitis and extrahepatic biliary atresia Recurrent and de novo giant cell hepatitis after orthotopic liver transplantation Hepatocellular carcinoma following neonatal hepatitis Congenital cirrhosis of the liver with kernicterus; report of two cases in siblings with a discussion of the relationship to so-called neonatal hepatitis and to iso-immunization disease. Iron storage disease in parents and sibs of infants with neonatal hemochromatosis: 30-year follow-up Neonatal hemochromatosis: report of successful orthotopic liver transplantation. Neonatal hemochromatosis associated with maternal autoantibodies against Ro/SS-A and La/SS-B ribonucleoproteins. Neonatal hemochromatosis: failure of deferoxamine therapy. Fetal liver disease may precede extrahepatic siderosis in neonatal hemochromatosis Neonatal hemochromatosis: diagnosis with MR imaging Familial neonatal hemochromatosis with survival Cytoferrin, maternofetal iron transport, and neonatal hemochromatosis Multiple malformations in neonatal hemochromatosis Faetal and neonatal hepatitis and its sequelae Idiopathic neonatal hemochromatosis in siblings. An inborn error of metabolism Perinatal idiopathic hemochromatosis: giant cell hepatitis interpreted as an inborn error of metabolism

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