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Terminology chevron_right Concepts chevron_right 716743006

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716743006
The component that hold information about this concept.
Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder)
Familial non-immune hyperthyroidism
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 hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder)

SCTID: 716743006, Primitive, Active


716743006|Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder)|
  • en Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor
  • en Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder)
  • en Familial non-autoimmune autosomal dominant hyperthyroidism
  • en Familial non-immune hyperthyroidism

716743006 |Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder)|

<<< 11164009 |Autosomal dominant hereditary disorder (disorder)| +
    34486009 |Hyperthyroidism (disorder)| +
    363104002 |Hereditary disorder of endocrine system (disorder)| :
        { 363698007 |Finding site (attribute)| = 69748006 |Thyroid structure (body structure)| }
        { 42752001 |Due to (attribute)| = 50375007 |Thyroid hormone responsiveness defect (disorder)| }
Active

3307393013 - Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (en) View

3307393013
en
Synonym (core metadata concept)
Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

3307392015 - Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder) (en) View

3307392015
en
Fully specified name (core metadata concept)
Familial hyperthyroidism due to mutation in thyroid stimulating hormone receptor (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3307395018 - Familial non-autoimmune autosomal dominant hyperthyroidism (en) View

3307395018
en
Synonym (core metadata concept)
Familial non-autoimmune autosomal dominant hyperthyroidism
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3307394019 - Familial non-immune hyperthyroidism (en) View

3307394019
en
Synonym (core metadata concept)
Familial non-immune hyperthyroidism
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

Relationship (7112351026) - 716743006 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6571450024) - 716743006 -> 50375007 (42752001) View

42752001 |Due to (attribute)|
50375007 |Thyroid hormone responsiveness defect (disorder)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6571454026) - 716743006 -> 69748006 (363698007) View

363698007 |Finding site (attribute)|
69748006 |Thyroid structure (body structure)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (7112352022) - 716743006 -> 69748006 (363698007) View

363698007 |Finding site (attribute)|
69748006 |Thyroid structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6571451023) - 716743006 -> 11164009 (116680003) View

116680003 |Is a (attribute)|
11164009 |Autosomal dominant hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6571452027) - 716743006 -> 34486009 (116680003) View

116680003 |Is a (attribute)|
34486009 |Hyperthyroidism (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6571453021) - 716743006 -> 363104002 (116680003) View

116680003 |Is a (attribute)|
363104002 |Hereditary disorder of endocrine system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

11164009 View

11164009
Autosomal dominant hereditary disorder (disorder)
Ad - autosomal dominant
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

34486009 View

34486009
Hyperthyroidism (disorder)
Cường giáp
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

363104002 View

363104002
Hereditary disorder of endocrine system (disorder)
Hereditary disorder of endocrine system
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (bd78e97f-c8a7-5f35-b1c1-973a9e9469cd) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E05.8
TRUE
ALWAYS E05.8
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)|
esc