SNOMED Clinical Terms - Neonatal hemochromatosis - Terms

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Preferred Name	Neonatal hemochromatosis
Synonyms	Idiopathic neonatal hemochromatosis Neonatal giant cell hepatitis Neonatal haemochromatosis Idiopathic neonatal haemochromatosis Neonatal hemochromatosis (disorder)
ID	6160004
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/6160004
CONCEPTSTATUS	0
CTV3ID	X40QQ
has_causative_agent	Iron AND/OR iron compound
has_clinical_course	Courses
has_episodicity	Episodicities
has_severity	Severities
isa	Hemochromatosis Neonatal disorder
ISPRIMITIVE	0
occurs_in	Neonatal
same_as	Neonatal giant cell hepatitis
Semantic_Type	Disease or Syndrome
SNOMEDID	D6-31214
SYNONYM FN	Neonatal hemochromatosis (disorder)
SYNONYM PTGB	Neonatal haemochromatosis
SYNONYM SY	Idiopathic neonatal hemochromatosis Neonatal giant cell hepatitis
SYNONYM SYGB	Idiopathic neonatal haemochromatosis
TUI	T047
UMLS_CUI	C0268059

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://www.orphanet.org/rdfns#pat_id_504	Experimental Factor Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X40QQ	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU023490	Online Mendelian Inheritance in Man	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X307p	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0268059	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X40QQ	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0268059	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X307p	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU023490	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0268059	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/231100	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0268059	skos:closeMatch	loom	04/02/13	View Notes
http://www.orphanet.org/rdfns#pat_id_504	Orphanet Ontology of Rare Diseases	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://bioonto.de/mesh.owl#C536394	OWL Version of MeSH	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MSH/C536394	Medical Subject Headings (MeSH)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MSH/C536394	Medical Subject Headings (MeSH)	NLM UMLS (CUI)	CUI: C0268059	skos:closeMatch	loom	04/02/13	View Notes

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