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Liddle syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0008323

A rare genetic form of low-renin hypertension characterized by hypertension associated with decreased plasma levels of potassium and aldosterone. [ Orphanet:526 ]

Synonyms: Liddle's syndrome pseudoaldosteronism Liddle syndrome

This is just here as a test because I lose it

Term information

database cross reference
  • MedDRA:10052313 (Orphanet:526/e)
  • Orphanet:526 (OMIM:177200)
  • NCIT:C84827 (MONDO:equivalentTo)
  • NORD:2034 (MONDO:NORD)
  • OMIMPS:177200 (MONDO:equivalentTo)
  • GARD:7381 (Orphanet:526)
  • DOID:0050477 (MONDO:equivalentTo)
  • MedDRA:10037113 (Orphanet:526/e)
  • MESH:D056929 (Orphanet:526/e)
  • SCTID:707747007 (MONDO:equivalentTo)
  • UMLS:C0221043 (Orphanet:526/e)
Subsets

gard_rare, ordo_disease, rare, nord_rare, orphanet_rare, clingen

closeMatch

http://identifiers.org/meddra/10052313

http://identifiers.org/meddra/10037113

exactMatch

http://purl.obolibrary.org/obo/NCIT_C84827

http://purl.obolibrary.org/obo/DOID_0050477

http://www.orpha.net/ORDO/Orphanet_526

https://omim.org/phenotypicSeries/PS177200

http://linkedlifedata.com/resource/umls/id/C0221043

http://identifiers.org/snomedct/707747007

http://identifiers.org/mesh/D056929

has narrow synonym

pseudohyperaldosteronism type 1

id

MONDO:0008323

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0008323

https://rarediseases.info.nih.gov/diseases/7381/liddle-syndrome