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Terminology chevron_right Concepts chevron_right 721838005

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721838005
The component that hold information about this concept.
Familial hypertryptophanemia (disorder)
Familial hypertryptophanemia
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

Familial hypertryptophanemia (disorder)

SCTID: 721838005, Primitive, Active


721838005|Familial hypertryptophanemia (disorder)|
  • en Familial hypertryptophanaemia
  • en Familial hypertryptophanemia
  • en Familial hypertryptophanemia (disorder)

721838005 |Familial hypertryptophanemia (disorder)|

<<< 85995004 |Autosomal recessive hereditary disorder (disorder)| +
    111941005 |Familial disease (disorder)| +
    237925006 |Tryptophanemia (disorder)|
Active

3326207016 - Familial hypertryptophanaemia (en) View

3326207016
en
Synonym (core metadata concept)
Familial hypertryptophanaemia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3326200019 - Familial hypertryptophanemia (en) View

3326200019
en
Synonym (core metadata concept)
Familial hypertryptophanemia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3326199017 - Familial hypertryptophanemia (disorder) (en) View

3326199017
en
Fully specified name (core metadata concept)
Familial hypertryptophanemia (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (6761159025) - 721838005 -> 85995004 (116680003) View

116680003 |Is a (attribute)|
85995004 |Autosomal recessive hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6761160024) - 721838005 -> 111941005 (116680003) View

116680003 |Is a (attribute)|
111941005 |Familial disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6761161023) - 721838005 -> 237925006 (116680003) View

116680003 |Is a (attribute)|
237925006 |Tryptophanemia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

85995004 View

85995004
Autosomal recessive hereditary disorder (disorder)
Hereditary disorder trait, nos
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

111941005 View

111941005
Familial disease (disorder)
Familial disease
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

237925006 View

237925006
Tryptophanemia (disorder)
Tryptophanemia
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (671a4221-a528-54f2-bc5c-655d88d01e84) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E70.8
TRUE
ALWAYS E70.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
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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