- Concept UI
- M0532727
- Scope Note
- An hereditary hemolytic uremic syndrome associated with variations in the gene that encodes COMPLEMENT FACTOR H, or the related proteins CFHR1 and CFHR3. Disease often progresses to CHRONIC KIDNEY FAILURE without the prodromal symptoms of ENTEROCOLITIS and DIARRHEA that characterize typical hemolytic uremic syndrome.
- Terms
-
Atypical Hemolytic Uremic Syndrome
Preferred Term
Term UI
T854025
Date01/23/2014
LexicalTag
NON
ThesaurusID
ORD (2010)
-
Atypical Hemolytic-Uremic Syndrome
Term UI
T840957
Date04/18/2013
LexicalTag
NON
ThesaurusID
GHR (2014)
-
Non-Stx-Hus
Term UI
T840959
Date04/18/2013
LexicalTag
ABX
ThesaurusID
GHR (2014)
-
Hemolytic Uremic Syndrome, Atypical
Term UI
T854026
Date01/23/2014
LexicalTag
NON
ThesaurusID
ORD (2010)
-
Nonenteropathic HUS
Term UI
T854027
Date01/23/2014
LexicalTag
NON
ThesaurusID
GHR (2014)
-
Non-Shiga-Like Toxin-Associated HUS
Term UI
T854034
Date01/23/2014
LexicalTag
NON
ThesaurusID
GHR (2014)