SNOMED Clinical Terms - Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

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Preferred Name	Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction
Synonyms	Herrmann syndrome Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction (disorder)
ID	237612000
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/237612000
CONCEPTSTATUS	0
CTV3ID	X40JR
has_clinical_course	Courses
has_episodicity	Episodicities
has_finding_site	Endocrine pancreatic structure
has_severity	Severities
isa	Disorder of endocrine pancreas Multisystem disorder
ISPRIMITIVE	1
Semantic_Type	Disease or Syndrome
SNOMEDID	DF-0009D
SYNONYM FN	Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction (disorder)
SYNONYM SY	Herrmann syndrome
TUI	T047
UMLS_CUI	C1809475

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.bioontology.org/ontology/RCD/X40JR	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://bioonto.de/mesh.owl#C538113	OWL Version of MeSH	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MSH/C538113	Medical Subject Headings (MeSH)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X40JR	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C1809475	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/172500	Online Mendelian Inheritance in Man	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/172500	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C1809475	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MSH/C538113	Medical Subject Headings (MeSH)	NLM UMLS (CUI)	CUI: C1809475	skos:closeMatch	loom	04/02/13	View Notes

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