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Terminology chevron_right Concepts chevron_right 25765006

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  • Language with ID “edb06b02-cf19-5fdd-bf79-e1ce3a4384f3” doesn’t exist. Perhaps it was deleted?
The component that hold information about this concept.
Neonatal iminoglycinuria (disorder)
Neonatal iminoglycinuria
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Neonatal iminoglycinuria (disorder)

SCTID: 25765006, Defined, Active


25765006|Neonatal iminoglycinuria (disorder)|
  • en Neonatal iminoglycinuria
  • en Neonatal iminoglycinuria (disorder)

25765006 |Neonatal iminoglycinuria (disorder)|

=== 84121007 |Iminoglycinuria (disorder)| +
    363224005 |Neonatal renal disorder (disorder)| +
    736652002 |Neonatal metabolic disorder (disorder)| :
        { 246454002 |Occurrence (attribute)| = 255407002 |Neonatal (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 64033007 |Kidney structure (body structure)| }
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