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Terminology chevron_right Concepts chevron_right 715436007

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The component that hold information about this concept.
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder)
Cerebellar hypoplasia and tapetoretinal degeneration
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder)

SCTID: 715436007, Primitive, Active


715436007|Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder)|
  • en Cerebellar hypoplasia and tapetoretinal degeneration
  • en Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration
  • en Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder)

715436007 |Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder)|

<<< 16026008 |Congenital cerebellar hypoplasia (disorder)| +
    363235000 |Hereditary disorder of nervous system (disorder)| +
    363343008 |Hereditary disorder of the visual system (disorder)| +
    363070008 |Developmental hereditary disorder (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 55199003 |Hypoplasia (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 113305005 |Cerebellar structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 49549006 |Structure of visual system (body structure)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
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