Congenital melanosis 86042009 SNOMED CT code SNOMED code 86042009 name Congenital melanosis status active date introduced 2002-01-31 fully specified name(s) Congenital melanosis (disorder) synonyms Congenital melanosis attributes - group1 Occurrence Congenital 255399007 Associated morphology Melanosis 48010006 parents children Acromelanosis 239089006 Arterial dissection and lentiginosis syndrome 720512007 Centrofacial lentiginosis syndrome 18822004 Congenital melanosis of sclera 51174006 Dermal melanocytic hamartoma 897554004 Familial generalized lentiginosis 765195000 Hereditary benign acanthosis nigricans 205583005 Hereditary benign acanthosis nigricans with insulin resistance 237606005 Melanosis oculi 45795007 Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome 764995008 Peutz-Jeghers syndrome 54411001 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Melanosis 414662006 Congenital melanosis 86042009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital melanosis 86042009 ancestors sorted most to least specific
cpt crosswalks Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.
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