autosomaal recessieve hereditaire aandoening
familiaire hypomagnesiëmie met hypercalciurie
hereditaire nefropathie
nefrocalcinose
||||
familiaire primaire hypomagnesiëmie met hypercalciurie en nefrocalcinose (aandoening)
familiaire primaire hypomagnesiëmie met hypercalciurie en nefrocalcinose
FHHNC
familiale primaire hypomagnesiëmie met hypercalciurie en nephrocalcinosis
syndroom van Michellis-Castrillo
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
FHHNC - familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
Michellis Castrillo syndrome
Primary hypomagnesemia with hypercalciuria and nephrocalcinosis
Id1304111007
StatusPrimitive
Associated morphologypathologische calcificatie
Finding sitenierparenchym
Has interpretationboven referentiebereik
Interpretsbepalen van calcium in urine
SNOMED CT to ICD-10 extended map
TargetE83.4
RuleTRUE
AdviceALWAYS E83.4 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
TargetE83.5
RuleTRUE
AdviceALWAYS E83.5
CorrelationSNOMED CT source code to target map code correlation not specified
TargetN29.8
RuleTRUE
AdviceALWAYS N29.8 | THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE
CorrelationSNOMED CT source code to target map code correlation not specified
|
familiaire hypomagnesiëmie met hypercalciurie en nefrocalcinose met ernstige oculaire betrokkenheid
familiaire primaire hypomagnesiëmie met hypercalciurie en nefrocalcinose zonder ernstige oculaire betrokkenheid