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Terminology chevron_right Concepts chevron_right 789063000

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789063000
The component that hold information about this concept.
Primary hyperaldosteronism, seizures, neurological abnormalities syndrome (disorder)
Primary hyperaldosteronism, seizures, neurological abnormalities syndrome
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

Primary hyperaldosteronism, seizures, neurological abnormalities syndrome (disorder)

SCTID: 789063000, Primitive, Active


789063000|Primary hyperaldosteronism, seizures, neurological abnormalities syndrome (disorder)|
  • en Primary hyperaldosteronism, seizures, neurological abnormalities syndrome
  • en Primary hyperaldosteronism, seizures, neurological abnormalities syndrome (disorder)

789063000 |Primary hyperaldosteronism, seizures, neurological abnormalities syndrome (disorder)|

<<< 11164009 |Autosomal dominant hereditary disorder (disorder)| +
    128613002 |Seizure disorder (disorder)| +
    190507007 |Primary hyperaldosteronism (disorder)| +
    363104002 |Hereditary disorder of endocrine system (disorder)| +
    363235000 |Hereditary disorder of nervous system (disorder)| :
        { 363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 68594002 |Adrenal cortex structure (body structure)| }
Active

3786588011 - Primary hyperaldosteronism, seizures, neurological abnormalities syndrome (en) View

3786588011
en
Synonym (core metadata concept)
Primary hyperaldosteronism, seizures, neurological abnormalities syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3786587018 - Primary hyperaldosteronism, seizures, neurological abnormalities syndrome (disorder) (en) View

3786587018
en
Fully specified name (core metadata concept)
Primary hyperaldosteronism, seizures, neurological abnormalities syndrome (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (12876751020) - 789063000 -> 363104002 (116680003) View

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

Relationship (12101208020) - 789063000 -> 12738006 (363698007) View

363698007 |Finding site (attribute)|
12738006 |Brain structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12101209028) - 789063000 -> 128613002 (116680003) View

116680003 |Is a (attribute)|
128613002 |Seizure disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12101210022) - 789063000 -> 68594002 (363698007) View

363698007 |Finding site (attribute)|
68594002 |Adrenal cortex structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12101211021) - 789063000 -> 11164009 (116680003) View

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

Relationship (12101212025) - 789063000 -> 363235000 (116680003) View

116680003 |Is a (attribute)|
363235000 |Hereditary disorder of nervous system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12101213024) - 789063000 -> 190507007 (116680003) View

116680003 |Is a (attribute)|
190507007 |Primary hyperaldosteronism (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

128613002 View

128613002
Seizure disorder (disorder)
Bệnh co giật
900000000000073002 |Sufficiently defined by necessary conditions definition status (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

190507007 View

190507007
Primary hyperaldosteronism (disorder)
Conn syndrome
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

363235000 View

363235000
Hereditary disorder of nervous system (disorder)
Hereditary disorder of nervous system
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (93d848ad-3077-5326-9210-d546ae520360) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E26.0
TRUE
ALWAYS E26.0 | 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)|
esc