Loading...
dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 702379005

Production
add
702379005
The component that hold information about this concept.
Hypomyelination and congenital cataract (disorder)
Hypomyelination and congenital cataract
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

Hypomyelination and congenital cataract (disorder)

SCTID: 702379005, Primitive, Active


702379005|Hypomyelination and congenital cataract (disorder)|
  • en Hypomyelination and congenital cataract
  • en Hypomyelination and congenital cataract (disorder)
  • en Hcc - hypomyelination and congenital cataract

702379005 |Hypomyelination and congenital cataract (disorder)|

<<< 363235000 |Hereditary disorder of nervous system (disorder)| +
    22811006 |Leukoencephalopathy (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| :
        { 363698007 |Finding site (attribute)| = 68523003 |Cerebral white matter structure (body structure)| }
Active

2995422017 - Hypomyelination and congenital cataract (en) View

2995422017
en
Synonym (core metadata concept)
Hypomyelination and congenital cataract
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

2995853012 - Hypomyelination and congenital cataract (disorder) (en) View

2995853012
en
Fully specified name (core metadata concept)
Hypomyelination and congenital cataract (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

2995368018 - HCC - hypomyelination and congenital cataract (en) View

2995368018
en
Synonym (core metadata concept)
HCC - hypomyelination and congenital cataract
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

22811006 View

22811006
Leukoencephalopathy (disorder)
Leucoencephalopathy
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

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 (ee15cddd-8cd1-5fa5-b3c0-f0e97ae6ce10) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G37.8
TRUE
ALWAYS G37.8
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