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Terminology chevron_right Concepts chevron_right 18417009

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The component that hold information about this concept.
Oligomeganephronic hypoplasia of kidney (disorder)
Oligomeganephronia
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Oligomeganephronic hypoplasia of kidney (disorder)

SCTID: 18417009, Primitive, Active


18417009|Oligomeganephronic hypoplasia of kidney (disorder)|
  • en Oligomeganephronia
  • en Oligomeganephronic hypoplasia
  • en Oligomeganephronic hypoplasia of kidney
  • en Oligomeganephronic hypoplasia of kidney (disorder)

18417009 |Oligomeganephronic hypoplasia of kidney (disorder)|

<<< 32659003 |Congenital hypoplasia of kidney (disorder)| +
    897175000 |Structural abnormality of nephron (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 1303291008 |Abnormal number (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 54018001 |Nephron structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 55199003 |Hypoplasia (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 64033007 |Kidney structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
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