Loading...
dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 774152007

Production
add
774152007
The component that hold information about this concept.
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies (disorder)
Retinal dystrophy with inner nuclear layer and ganglion cell anomalies
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

Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies (disorder)

SCTID: 774152007, Primitive, Active


774152007|Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies (disorder)|
  • en Retinal dystrophy with inner nuclear layer and ganglion cell anomalies
  • en Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies
  • en Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies (disorder)

774152007 |Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies (disorder)|

<<< 41799005 |Hereditary retinal dystrophy (disorder)| +
    11164009 |Autosomal dominant hereditary disorder (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)| }
Active

3728156012 - Retinal dystrophy with inner nuclear layer and ganglion cell anomalies (en) View

3728156012
en
Synonym (core metadata concept)
Retinal dystrophy with inner nuclear layer and ganglion cell anomalies
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

3728155011 - Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies (en) View

3728155011
en
Synonym (core metadata concept)
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3728157015 - Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies (disorder) (en) View

3728157015
en
Fully specified name (core metadata concept)
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

11164009 View

11164009
Autosomal dominant hereditary disorder (disorder)
Ad - autosomal dominant
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
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 (179c108f-e136-5f3a-aca4-11c821f563bf) 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)|
esc