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Terminology chevron_right Concepts chevron_right 65791008

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The component that hold information about this concept.
Adenine phosphoribosyltransferase (aprt) deficiency, japanese type (disorder)
Aprt deficiency, japanese type
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Adenine phosphoribosyltransferase (aprt) deficiency, japanese type (disorder)

SCTID: 65791008, Primitive, Active


65791008|Adenine phosphoribosyltransferase (aprt) deficiency, japanese type (disorder)|
  • en Adenine phosphoribosyltransferase deficiency, japanese type
  • en Adenine phosphoribosyltransferase deficiency, japanese type (disorder)
  • en Adenine phosphoribosyltransferase (aprt) deficiency, japanese type
  • en Aprt deficiency, japanese type

65791008 |Adenine phosphoribosyltransferase (aprt) deficiency, japanese type (disorder)|

<<< 124274002 |Deficiency of adenine phosphoribosyltransferase (disorder)|
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