SNOMED Clinical Terms - Holt-Oram syndrome - Terms

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Preferred Name	Holt-Oram syndrome
Synonyms	Atrio-digital syndrome Cardiac-limb syndrome Holt-Oram syndrome (disorder)
ID	19092004
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/19092004
CONCEPTSTATUS	0
CTV3ID	XU8oA
has_associated_morphology	Morphologically abnormal structure Congenital malformation
has_clinical_course	Courses
has_finding_site	Limb structure Heart structure
has_severity	Severities
isa	Congenital anomaly of limb Structural disorder of heart Multiple malformation syndrome with limb defect as major feature
ISPRIMITIVE	1
occurs_in	Congenital
same_as	Holt-Oram syndrome
Semantic_Type	Congenital Abnormality Disease or Syndrome
SNOMEDID	D4-00906
SYNONYM FN	Holt-Oram syndrome (disorder)
SYNONYM SY	Atrio-digital syndrome Cardiac-limb syndrome
TUI	T019 T047
UMLS_CUI	C0265264

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.bioontology.org/ontology/MDR/10050469	MedDRA	NLM UMLS (CUI)	CUI: C0265264	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/CSP/5002-0020	CRISP Thesaurus, 2006	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://bioonto.de/mesh.owl#C535326	OWL Version of MeSH	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/142900	Online Mendelian Inheritance in Man	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/CSP/5002-0020	CRISP Thesaurus, 2006	NLM UMLS (CUI)	CUI: C0265264	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q87.2	ICD10CM	NLM UMLS (CUI)	CUI: C0265264	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/PKy71	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0265264	skos:closeMatch	loom	04/02/13	View Notes
http://purl.org/skeletome/bonedysplasia#Holt-Oram_syndrome	Bone Dysplasia Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://www.orphanet.org/rdfns#pat_id_1023	Orphanet Ontology of Rare Diseases	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://www.co-ode.org/ontologies/galen#HoltOramSyndrome	Galen	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://www.orphanet.org/rdfns#pat_id_1023	Experimental Factor Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/PKy71	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MDR/10050469	MedDRA	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/142900	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0265264	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MSH/C535326	Medical Subject Headings (MeSH)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q87.2	ICD10CM	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MSH/C535326	Medical Subject Headings (MeSH)	NLM UMLS (CUI)	CUI: C0265264	skos:closeMatch	loom	04/02/13	View Notes

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