stoornis in lipidenmetabolisme
X-gebonden hereditaire aandoening
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OCRL inositol polyphosphate-5-phosphatase gene related phosphatidylinositol 4,5-bisphosphate 5-phosphatase deficiency (disorder)
OCRL gene related phosphatidylinositol 4,5-bisphosphate-5-phosphatase deficiency
OCRL inositol polyphosphate-5-phosphatase gene related phosphatidylinositol 4,5-bisphosphate 5-phosphatase deficiency
Id1399582000
StatusPrimitive
SNOMED CT to ICD-10 extended map
TargetE72.0
RuleTRUE
AdviceALWAYS E72.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
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Lowe-syndroom
ziekte van Dent type 2