Vision 3 Local Codes

The following SNOMED CT codes do not map to existing Read codes, Cegedim Healthcare Solutions have therefore created Vision 3 Local Codes, based on the Read code format, to enable you to both record and report on these new codes within Vision 3:

Latest Release

SNOMED CT Release v35.2

SNOMED CT Code

Description

Vision Local Code

Keyword(s)

Release

1464661000000106 Discussion about continuous glucose monitoring 67P6.00 CGM 35.2
1464651000000108 Discussion about flash glucose monitoring 67P7.00 FLASH 35.2
1464531000000102 Flash glucose monitoring declined 8IHT.00 FLASH 35.2
1464541000000106 Continuous glucose monitoring declined 8IHU.00

CGM

35.2
1464621000000103 Flash glucose monitoring stopped 8CTB.00 FLASH 35.2
1464641000000105 Continuous glucose monitoring stopped 8CTC.00 CGM 35.2
1464581000000103 Referral for continuous glucose monitoring 8HRI.00 CGM 35.2
1464571000000100 Referral for flash glucose monitoring 8HRJ.00 FLASH 35.2
1443921000000100 Edoxaban contraindicated 8IJ3.00 DOAC 35.2
1443911000000106 Edoxaban declined 8IHV.00 DOAC 35.2
1464371000000107 Edoxaban not tolerated 8I7b.00 DOAC 35.2
1423901000000106 Review of medical record relating to firearms licence 9Ej0.00 FIREARM 35.2
925221000000106 Familial hypercholesterolaemia comprehensive genetic test 4L4O.00 HYPERCHOL 35.2
163841000237109 Familial hypercholesterolaemia comprehensive genetic test result 4L4O000 HYPERCHOL 35.2
925211000000100 Familial hypercholesterolaemia targeted genetic test 4L4P.00 HYPERCHOL 35.2
163851000237107 Familial hypercholesterolaemia targeted genetic test result 4L4P000 HYPERCHOL 35.2
204871000237101 Apolipoprotein B gene mutation positive 4L13000 HYPERCHOL 35.2
204901000237101 Apolipoprotein E gene mutation positive 4L10000 HYPERCHOL 35.2
204881000237104 Proprotein convertase subtilisin-kexin type 9 gene mutation positive 4L12000 HYPERCHOL 35.2
204891000237102 Low density lipoprotein receptor gene mutation positive 4L14000 HYPERCHOL 35.2
204921000237108 Genetic variant of uncertain significance detected 4L4Q.00 GENETICVAR 35.2
204931000237105 Genetic variant causing familial hypercholesterolaemia not detected 4L4R.00 HYPERCHOL 35.2

Previous releases

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