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Terminology chevron_right Concepts chevron_right 65520001

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65520001
The component that hold information about this concept.
Primary hyperoxaluria, type i (disorder)
Ph i
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Primary hyperoxaluria, type i (disorder)

SCTID: 65520001, Primitive, Active


65520001|Primary hyperoxaluria, type i (disorder)|
  • en Alanine-glycoxylate aminotransferase deficiency
  • en Alanine-glyoxylate aminotransferase deficiency
  • en Glycolic aciduria
  • en 2-oxoglutarate glyoxylate carboligase deficiency
  • en Oxalosis type i
  • en Primary hyperoxaluria type i
  • en Primary hyperoxaluria, type i
  • en Primary hyperoxaluria, type i (disorder)

65520001 |Primary hyperoxaluria, type i (disorder)|

<<< 17901006 |Primary hyperoxaluria (disorder)| +
    238066006 |Loss of single peroxisomal function (disorder)| :
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 64033007 |Kidney structure (body structure)| }
Active

1232690010 - Alanine-glycoxylate aminotransferase deficiency (en) View

1232690010
en
Synonym (core metadata concept)
Alanine-glycoxylate aminotransferase deficiency
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

108863017 - Alanine-glyoxylate aminotransferase deficiency (en) View

108863017
en
Synonym (core metadata concept)
Alanine-glyoxylate aminotransferase deficiency
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

108862010 - Glycolic aciduria (en) View

108862010
en
Synonym (core metadata concept)
Glycolic aciduria
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

1232687016 - 2-Oxoglutarate glyoxylate carboligase deficiency (en) View

1232687016
en
Synonym (core metadata concept)
2-Oxoglutarate glyoxylate carboligase deficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

1232688014 - Oxalosis type I (en) View

1232688014
en
Synonym (core metadata concept)
Oxalosis type I
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

1232689018 - Primary hyperoxaluria type I (en) View

1232689018
en
Synonym (core metadata concept)
Primary hyperoxaluria type I
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

108864011 - PH I (en) View

108864011
en
Synonym (core metadata concept)
PH I
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
False

108861015 - Primary hyperoxaluria, type I (en) View

108861015
en
Synonym (core metadata concept)
Primary hyperoxaluria, type I
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

805032013 - Primary hyperoxaluria, type I (disorder) (en) View

805032013
en
Fully specified name (core metadata concept)
Primary hyperoxaluria, type I (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

17901006 View

17901006
Primary hyperoxaluria (disorder)
Primary oxalosis
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

238066006 View

238066006
Loss of single peroxisomal function (disorder)
Loss of single peroxisomal function
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (7a64896f-4676-5745-a1b9-efba38cf73af) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E74.8
TRUE
ALWAYS E74.8
447561005 |Snomed ct source code to target map code correlation not specified (foundation metadata concept)|
447637006 |Map source concept is properly classified (foundation metadata concept)|
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