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Terminology chevron_right Concepts chevron_right 413356003

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413356003
The component that hold information about this concept.
4-hydroxyphenylpyruvate dioxygenase deficiency (disorder)
4-hydroxyphenylpyruvate dioxygenase 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

4-hydroxyphenylpyruvate dioxygenase deficiency (disorder)

SCTID: 413356003, Primitive, Active


413356003|4-hydroxyphenylpyruvate dioxygenase deficiency (disorder)|
  • en 4-hydroxyphenylpyruvate dioxygenase deficiency
  • en 4-hydroxyphenylpyruvate dioxygenase deficiency (disorder)
  • en 4-hydroxyphenylpyruvate hydroxylase deficiency

413356003 |4-hydroxyphenylpyruvate dioxygenase deficiency (disorder)|

<<< 37200009 |Disorder of tyrosine metabolism (disorder)| +
    78548001 |Enzymopathy (disorder)|
Active

2533518013 - 4-Hydroxyphenylpyruvate dioxygenase deficiency (en) View

2533518013
en
Synonym (core metadata concept)
4-Hydroxyphenylpyruvate dioxygenase deficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

2530082011 - 4-Hydroxyphenylpyruvate dioxygenase deficiency (disorder) (en) View

2530082011
en
Fully specified name (core metadata concept)
4-Hydroxyphenylpyruvate dioxygenase deficiency (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

2537080017 - 4-Hydroxyphenylpyruvate hydroxylase deficiency (en) View

2537080017
en
Synonym (core metadata concept)
4-Hydroxyphenylpyruvate hydroxylase deficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

Relationship (2684489025) - 413356003 -> 37200009 (116680003) View

116680003 |Is a (attribute)|
37200009 |Disorder of tyrosine metabolism (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (2684490023) - 413356003 -> 78548001 (116680003) View

116680003 |Is a (attribute)|
78548001 |Enzymopathy (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

37200009 View

37200009
Disorder of tyrosine metabolism (disorder)
Disorder of tyrosine metabolism
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

78548001 View

78548001
Enzymopathy (disorder)
Enzymopathy
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

414380008 View

414380008
Hawkinsinuria (disorder)
Hawkinsinuria
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

415764005 View

415764005
Tyrosinemia type iii (disorder)
Tyrosinemia type 3
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (9f6e3a48-e4f6-5903-974d-10c6ed0e03c9) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E70.2
TRUE
ALWAYS E70.2
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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