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Terminology chevron_right Concepts chevron_right 1186807002

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1186807002
The component that hold information about this concept.
Hereditary growth hormone deficiency (disorder)
Hereditary growth hormone 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

Hereditary growth hormone deficiency (disorder)

SCTID: 1186807002, Defined, Active


1186807002|Hereditary growth hormone deficiency (disorder)|
  • en Hereditary growth hormone deficiency
  • en Hereditary growth hormone deficiency (disorder)

1186807002 |Hereditary growth hormone deficiency (disorder)|

=== 363104002 |Hereditary disorder of endocrine system (disorder)| +
    363235000 |Hereditary disorder of nervous system (disorder)| +
    397827003 |Growth hormone deficiency (disorder)| :
        { 363698007 |Finding site (attribute)| = 52618001 |Structure of pars distalis of pituitary (body structure)| }
Active

4667739016 - Hereditary growth hormone deficiency (en) View

4667739016
en
Synonym (core metadata concept)
Hereditary growth hormone deficiency
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

4667738012 - Hereditary growth hormone deficiency (disorder) (en) View

4667738012
en
Fully specified name (core metadata concept)
Hereditary growth hormone deficiency (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

397827003 View

397827003
Growth hormone deficiency (disorder)
Thiếu hormon tăng trưởng
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

1220595008 View

1220595008
Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome (disorder)
Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

724385009 View

724385009
Growth delay due to insulin-like growth factor type 1 deficiency (disorder)
Primary insulin-like growth factor deficiency
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (36a2872b-6e35-5249-ad0b-8734a0aa98db) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E23.0
TRUE
ALWAYS E23.0
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)|
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