Preferred Name

Congenital porphyria
Synonyms

Congenital porphyria (disorder)
ID

190913009
Full Id

http://purl.bioontology.org/ontology/SNOMEDCT/190913009
CONCEPTSTATUS

0
CTV3ID

C3710
has_clinical_course

Courses
has_severity

Severities
isa

Congenital disease

Inherited disorder of porphyrin metabolism

Porphyria
ISPRIMITIVE

0
occurs_in

Congenital
Semantic_Type

Disease or Syndrome
SNOMEDID

D6-0000F
SYNONYM FN

Congenital porphyria (disorder)
TUI

T047
UMLS_CUI

C0162530
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Mapping To Ontology Source Comment Relationship Added By Added On Notes
http://purl.bioontology.org/ontology/CSP/1849-7617 CRISP Thesaurus, 2006 NLM UMLS (CUI) CUI: C0162530 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/NDFRT/N0000003526 National Drug File NLM UMLS (CUI) CUI: C0162530 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MSH/D017092 Medical Subject Headings (MeSH) NLM UMLS (CUI) CUI: C0162530 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MDR/10015288 MedDRA NLM UMLS (CUI) CUI: C0162530 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/ICD10/E80.0 ICD10 NLM UMLS (CUI) CUI: C0162530 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/ICD10CM/E80.0 ICD10CM NLM UMLS (CUI) CUI: C0162530 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/263700 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C0162530 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/C3710 Read Codes, Clinical Terms Version 3 (CTV3) NLM UMLS (CUI) CUI: C0162530 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/C3710 Read Codes, Clinical Terms Version 3 (CTV3) NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/X40WR Read Codes, Clinical Terms Version 3 (CTV3) NLM UMLS (CUI) CUI: C0162530 skos:closeMatch loom 04/02/13 View Notes

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