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Terminology chevron_right Concepts chevron_right 721236002

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721236002
The component that hold information about this concept.
Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme a dehydrogenase deficiency (disorder)
Hyperinsulinism due to short chain 3-hydroxylacyl-coa dehydrogenase deficiency
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme a dehydrogenase deficiency (disorder)

SCTID: 721236002, Defined, Active


721236002|Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme a dehydrogenase deficiency (disorder)|
  • vi Tăng insulin máu do thiếu hụt 3-hydroxyacyl-coenzyme a dehydrogenase  chuỗi ngắn
  • en Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme a dehydrogenase deficiency
  • en Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme a dehydrogenase deficiency (disorder)
  • en Hyperinsulinism due to short chain 3-hydroxylacyl-coa dehydrogenase deficiency

721236002 |Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme a dehydrogenase deficiency (disorder)|

=== 66091009 |Congenital disease (disorder)| +
    42357009 |Disorder of digestive system specific to fetus or newborn (disorder)| +
    363080007 |Digestive system hereditary disorder (disorder)| +
    363104002 |Hereditary disorder of endocrine system (disorder)| +
    1363361006 |Diazoxide-sensitive diffuse hyperinsulinism (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| :
        { 363698007 |Finding site (attribute)| = 78696007 |Endocrine pancreatic structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 42752001 |Due to (attribute)| = 237998000 |Short chain 3-hydroxyacyl-coa dehydrogenase deficiency (disorder)| }
Active

456131000003113 - tăng insulin máu do thiếu hụt 3-hydroxyacyl-coenzyme A dehydrogenase  chuỗi ngắn (vi) View

456131000003113
vi
Synonym (core metadata concept)
tăng insulin máu do thiếu hụt 3-hydroxyacyl-coenzyme A dehydrogenase  chuỗi ngắn
900000000000448009 |Entire term case insensitive (core metadata concept)|
None
True

3324734017 - Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (en) View

3324734017
en
Synonym (core metadata concept)
Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

3324733011 - Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (disorder) (en) View

3324733011
en
Fully specified name (core metadata concept)
Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

3324735016 - Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency (en) View

3324735016
en
Synonym (core metadata concept)
Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

Relationship (6754433022) - 721236002 -> 83469008 (116680003) View

116680003 |Is a (attribute)|
83469008 |Hyperinsulinism (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (16329796027) - 721236002 -> 1363361006 (116680003) View

116680003 |Is a (attribute)|
1363361006 |Diazoxide-sensitive diffuse hyperinsulinism (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15880906029) - 721236002 -> 42357009 (116680003) View

116680003 |Is a (attribute)|
42357009 |Disorder of digestive system specific to fetus or newborn (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12876701026) - 721236002 -> 66091009 (116680003) View

116680003 |Is a (attribute)|
66091009 |Congenital disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6754432028) - 721236002 -> 237998000 (42752001) View

42752001 |Due to (attribute)|
237998000 |Short chain 3-hydroxyacyl-coa dehydrogenase deficiency (disorder)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6754437023) - 721236002 -> 78696007 (363698007) View

363698007 |Finding site (attribute)|
78696007 |Endocrine pancreatic structure (body structure)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (7112442024) - 721236002 -> 255399007 (246454002) View

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

Relationship (7112443025) - 721236002 -> 78696007 (363698007) View

363698007 |Finding site (attribute)|
78696007 |Endocrine pancreatic structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6754434027) - 721236002 -> 85995004 (116680003) View

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

Relationship (6754435026) - 721236002 -> 363080007 (116680003) View

116680003 |Is a (attribute)|
363080007 |Digestive system hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6754436025) - 721236002 -> 363104002 (116680003) View

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

1363361006 View

1363361006
Diazoxide-sensitive diffuse hyperinsulinism (disorder)
Diazoxide-sensitive diffuse hyperinsulinism
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

42357009 View

42357009
Disorder of digestive system specific to fetus or newborn (disorder)
Perinatal digestive system disorders
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

66091009 View

66091009
Congenital disease (disorder)
Congenital disease
900000000000073002 |Sufficiently defined by necessary conditions definition status (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

363080007 View

363080007
Digestive system hereditary disorder (disorder)
Digestive system hereditary disorder
900000000000073002 |Sufficiently defined by necessary conditions 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 (9cfc9781-b3de-56e7-b9c6-6a60102fd8ae) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E71.3
TRUE
ALWAYS E71.3 | 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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