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SNOMED CT code SNOMED code 367601000119103 name Hereditary amyloidosis status active date introduced 2017-07-31 fully specified name(s) Hereditary amyloidosis (disorder) synonyms Hereditary amyloidosis attributes - group1 Associated morphology Amyloid deposition 68790008 parents children AGel amyloidosis 783160006 Autosomal dominant beta2-microglobulinic amyloidosis 722292000 Familial amyloid nephropathy with urticaria AND deafness 15123008 Familial amyloid polyneuropathy 42295001 Gelatinous droplike corneal dystrophy 419900000 Hereditary cerebrovascular amyloidosis 237867001 Hereditary oculoleptomeningeal amyloid angiopathy 43532007 Hereditary systemic amyloidosis 107311000119104 Heredofamilial systemic amyloidosis affecting skin 402459005 ITM2B-related amyloidosis 1187126002 Lattice corneal dystrophy Type II 419087002 removed: 2020-01-31 Localized hereditary amyloidosis 237869003 Prion protein systemic amyloidosis 733422008 Transthyretin related familial amyloid cardiomyopathy 715655000 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 64572001 362975008 17602002 367601000119103 138875005 404684003 64572001 782964007 32895009 367601000119103 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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