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Terminology chevron_right Concepts chevron_right 698848005

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698848005
The component that hold information about this concept.
Hereditary retinal dystrophy primarily involving sensory retina (disorder)
Inherited retinal dystrophy primarily involving sensory retina
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

Hereditary retinal dystrophy primarily involving sensory retina (disorder)

SCTID: 698848005, Primitive, Active


698848005|Hereditary retinal dystrophy primarily involving sensory retina (disorder)|
  • en Hereditary retinal dystrophy primarily involving sensory retina
  • en Hereditary retinal dystrophy primarily involving sensory retina (disorder)
  • en Inherited retinal dystrophy primarily involving sensory retina

698848005 |Hereditary retinal dystrophy primarily involving sensory retina (disorder)|

<<< 41799005 |Hereditary retinal dystrophy (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)| }
Active

2981458015 - Hereditary retinal dystrophy primarily involving sensory retina (en) View

2981458015
en
Synonym (core metadata concept)
Hereditary retinal dystrophy primarily involving sensory retina
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

2981483015 - Hereditary retinal dystrophy primarily involving sensory retina (disorder) (en) View

2981483015
en
Fully specified name (core metadata concept)
Hereditary retinal dystrophy primarily involving sensory retina (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

2981465011 - Inherited retinal dystrophy primarily involving sensory retina (en) View

2981465011
en
Synonym (core metadata concept)
Inherited retinal dystrophy primarily involving sensory retina
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

41799005 View

41799005
Hereditary retinal dystrophy (disorder)
Hereditary retinal dystrophy
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (bea8ac03-055c-543b-9a89-2b065aa5fdd2) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
H35.5
TRUE
ALWAYS H35.5
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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