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Terminology chevron_right Concepts chevron_right 15991002

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15991002
The component that hold information about this concept.
Severe steroid 21-hydroxylase deficiency (disorder)
Severe steroid 21-hydroxylase 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

Severe steroid 21-hydroxylase deficiency (disorder)

SCTID: 15991002, Primitive, Active


15991002|Severe steroid 21-hydroxylase deficiency (disorder)|
  • en Severe steroid 21-hydroxylase deficiency
  • en Severe steroid 21-hydroxylase deficiency (disorder)

15991002 |Severe steroid 21-hydroxylase deficiency (disorder)|

<<< 86095007 |Inborn error of metabolism (disorder)| +
    363104002 |Hereditary disorder of endocrine system (disorder)| +
    124221007 |Deficiency of steroid 21-monooxygenase (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| :
        { 363698007 |Finding site (attribute)| = 68594002 |Adrenal cortex structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
Active

27072017 - Severe steroid 21-hydroxylase deficiency (en) View

27072017
en
Synonym (core metadata concept)
Severe steroid 21-hydroxylase deficiency
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

742926010 - Severe steroid 21-hydroxylase deficiency (disorder) (en) View

742926010
en
Fully specified name (core metadata concept)
Severe steroid 21-hydroxylase deficiency (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (709339025) - 15991002 -> 68594002 (363698007) View

363698007 |Finding site (attribute)|
68594002 |Adrenal cortex structure (body structure)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (709341029) - 15991002 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (7112077026) - 15991002 -> 255399007 (246454002) View

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

Relationship (7112078020) - 15991002 -> 68594002 (363698007) View

363698007 |Finding site (attribute)|
68594002 |Adrenal cortex structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (1758019027) - 15991002 -> 24484000 (246112005) View

246112005 |Severity (attribute)|
24484000 |Severe (severity modifier) (qualifier value)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (172103027) - 15991002 -> 271077003 (116680003) View

116680003 |Is a (attribute)|
271077003 |Adrenal virilism (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (172105023) - 15991002 -> 60637003 (116680003) View

116680003 |Is a (attribute)|
60637003 |Congenital anomaly of adrenal gland (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (172100029) - 15991002 -> 363290007 (116680003) View

116680003 |Is a (attribute)|
363290007 |Reproductive system hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (709340028) - 15991002 -> 127944005 (363698007) View

363698007 |Finding site (attribute)|
127944005 |Entire endocrine gonad (body structure)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (172099021) - 15991002 -> 86095007 (116680003) View

116680003 |Is a (attribute)|
86095007 |Inborn error of metabolism (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (172101025) - 15991002 -> 363104002 (116680003) View

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

Relationship (172102021) - 15991002 -> 124221007 (116680003) View

116680003 |Is a (attribute)|
124221007 |Deficiency of steroid 21-monooxygenase (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (172104022) - 15991002 -> 85995004 (116680003) View

116680003 |Is a (attribute)|
85995004 |Autosomal recessive hereditary disorder (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

86095007 View

86095007
Inborn error of metabolism (disorder)
Inborn error of metabolism
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

124221007 View

124221007
Deficiency of steroid 21-monooxygenase (disorder)
21-hydroxylase deficiency
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 (e3523d7e-810a-552c-a416-467772ec9fa4) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E25.0
TRUE
ALWAYS E25.0
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