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tempi syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0017286

TEMPI syndrome is a rare multi-systemic disease characterized by the presence of Telangiectasias, Erythrocytosis with elevated erythropoietin levels, Monoclonal gammopathy, Perinephric-fluid collections, and Intrapulmonary shunting. [ Orphanet:284227 ]

Synonyms: telangiectasia-erythrocytosis-monoclonal gammopathy-perinephric-fluid collections-intrapulmonary shunting syndrome

This is just here as a test because I lose it

Term information

database cross reference
  • SCTID:718614004 (MONDO:equivalentTo)
  • MEDGEN:886502 (MONDO:equivalentTo)
  • UMLS:C3854394 (MONDO:equivalentTo)
  • Orphanet:284227 (MONDO:equivalentTo)
  • NCIT:C121656 (MONDO:equivalentTo)
  • GARD:10962 (MONDO:GARD)
Subsets

ordo_disorder, gard_rare, ordo_clinical_syndrome, rare, nord_rare, orphanet_rare

exactMatch

http://identifiers.org/snomedct/718614004

http://www.orpha.net/ORDO/Orphanet_284227

http://linkedlifedata.com/resource/umls/id/C3854394

http://purl.obolibrary.org/obo/NCIT_C121656

http://identifiers.org/medgen/886502

has related synonym

telangiectasia - erythrocytosis - monoclonal gammopathy - perinephric-fluid collections - intrapulmonary shunting

id

MONDO:0017286

seeAlso

https://rarediseases.info.nih.gov/diseases/10962/tempi-syndrome

Term relations