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Terminology chevron_right Concepts chevron_right 723828008

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723828008
The component that hold information about this concept.
Autosomal recessive bestrophinopathy (disorder)
Retinopathy burgess black type
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

Autosomal recessive bestrophinopathy (disorder)

SCTID: 723828008, Primitive, Active


723828008|Autosomal recessive bestrophinopathy (disorder)|
  • en Autosomal recessive bestrophinopathy
  • en Autosomal recessive bestrophinopathy (disorder)
  • en Retinopathy burgess black type

723828008 |Autosomal recessive bestrophinopathy (disorder)|

<<< 41799005 |Hereditary retinal dystrophy (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)| }
Active

3426299014 - Autosomal recessive bestrophinopathy (en) View

3426299014
en
Synonym (core metadata concept)
Autosomal recessive bestrophinopathy
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3426300018 - Autosomal recessive bestrophinopathy (disorder) (en) View

3426300018
en
Fully specified name (core metadata concept)
Autosomal recessive bestrophinopathy (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3426298018 - Retinopathy Burgess Black type (en) View

3426298018
en
Synonym (core metadata concept)
Retinopathy Burgess Black type
900000000000020002 |Only initial character 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

85995004 View

85995004
Autosomal recessive hereditary disorder (disorder)
Hereditary disorder trait, nos
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (e0fda8a2-d4c9-5d14-983a-81fc0e8a9048) View

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