Loading...
dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 410053003

Production
add
410053003
The component that hold information about this concept.
Clinical manifestation of enzyme deficiency (disorder)
Clinical manifestation of enzyme deficiency
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

Clinical manifestation of enzyme deficiency (disorder)

SCTID: 410053003, Primitive, Active


410053003|Clinical manifestation of enzyme deficiency (disorder)|
  • en Clinical manifestation of enzyme deficiency
  • en Clinical manifestation of enzyme deficiency (disorder)

410053003 |Clinical manifestation of enzyme deficiency (disorder)|

<<< 75934005 |Metabolic disease (disorder)| :
        { 42752001 |Due to (attribute)| = 78548001 |Enzymopathy (disorder)| }
Active

2471779019 - Clinical manifestation of enzyme deficiency (en) View

2471779019
en
Synonym (core metadata concept)
Clinical manifestation of enzyme deficiency
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

2465504016 - Clinical manifestation of enzyme deficiency (disorder) (en) View

2465504016
en
Fully specified name (core metadata concept)
Clinical manifestation of enzyme deficiency (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (2589233020) - 410053003 -> 78548001 (42752001) View

42752001 |Due to (attribute)|
78548001 |Enzymopathy (disorder)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (2542647025) - 410053003 -> 75934005 (116680003) View

116680003 |Is a (attribute)|
75934005 |Metabolic disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

75934005 View

75934005
Metabolic disease (disorder)
Bệnh chuyển hóa
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

410050000 View

410050000
Clinical manifestation of carnosinase deficiency (disorder)
Clinical manifestation of carnosinase deficiency
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

410055005 View

410055005
Hyperimidodipeptiduria due to proline dipeptidase deficiency (disorder)
Iminodipeptiduria
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

410056006 View

410056006
Tyrosinemia type i (disorder)
Tyrosinemia type 1
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

410058007 View

410058007
Histidinemia (disorder)
Histidinemia
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

410059004 View

410059004
Hydroxymethylglutaric aciduria (disorder)
Hmg-coa lyase deficiency
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

314467007 View

314467007
Gyrate atrophy (disorder)
Gyrate atrophy
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (9960f602-681d-5495-b949-6aea1bc2bf4f) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
-
TRUE
MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
447561005 |Snomed ct source code to target map code correlation not specified (foundation metadata concept)|
447638001 |Map source concept cannot be classified with available data (foundation metadata concept)|
esc