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Complicated hereditary spastic paraplegia 230261006 SNOMED CT code SNOMED code 230261006 name Complicated hereditary spastic paraplegia status active date introduced 2002-01-31 fully specified name(s) Complicated hereditary spastic paraplegia (disorder) synonyms Complicated hereditary spastic paraplegia attributes - group2 Clinical course Progressive 255314001 attributes - group1 Associated morphology Degenerative abnormality 107669003 Finding site Spinal cord structure 2748008 attributes - group4 Interprets Movement 255324009 attributes - group5 Finding site Right lower extremity structure 62175007 attributes - group6 Finding site Left lower extremity structure 32153003 attributes - group3 Interprets Movement observable 363847004 Has interpretation Absent 2667000 parents Hereditary spastic paraplegia 39912006 children Autosomal dominant complex hereditary spastic paraplegia 1259038005 Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction 1186734006 Autosomal recessive spastic paraplegia type 11 715491000 Autosomal recessive spastic paraplegia type 14 783094006 Autosomal recessive spastic paraplegia type 15 764686003 Autosomal recessive spastic paraplegia type 18 732932004 Autosomal recessive spastic paraplegia type 21 764734003 Autosomal recessive spastic paraplegia type 23 726608002 Autosomal recessive spastic paraplegia type 25 732933009 Autosomal recessive spastic paraplegia type 26 726607007 Autosomal recessive spastic paraplegia type 32 726606003 Autosomal recessive spastic paraplegia type 35 764688002 Autosomal recessive spastic paraplegia type 39 719103009 Autosomal recessive spastic paraplegia type 43 764736001 Autosomal recessive spastic paraplegia type 44 723821002 Autosomal recessive spastic paraplegia type 46 723822009 Autosomal recessive spastic paraplegia type 53 723823004 Autosomal recessive spastic paraplegia type 54 723824005 Autosomal recessive spastic paraplegia type 58 770720005 Autosomal recessive spastic paraplegia type 59 773425000 Autosomal recessive spastic paraplegia type 60 782746009 Autosomal recessive spastic paraplegia type 61 726611001 Autosomal recessive spastic paraplegia type 63 726610000 Autosomal recessive spastic paraplegia type 64 726609005 Autosomal recessive spastic paraplegia type 66 782747000 Autosomal recessive spastic paraplegia type 67 766767001 Autosomal recessive spastic paraplegia type 69 782725000 Autosomal recessive spastic paraplegia type 70 770724001 Autosomal recessive spastic paraplegia type 75 1187470001 Autosomal recessive spastic paraplegia type 76 1172631001 Autosomal recessive spastic paraplegia type 78 1177168007 Autosomal recessive spastic paraplegia type 9B 1187467000 Hereditary sensory and autonomic neuropathy due to TECPR2 mutation 783198006 Hereditary sensory and autonomic neuropathy with spastic paraplegia 717827000 Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome 1172590009 MT-ATP6-related mitochondrial spastic paraplegia 778048001 Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome 1173998003 Severe intellectual disability and progressive spastic paraplegia 778011005 Spastic paraplegia, facial cutaneous lesion syndrome 763403007 Spastic paraplegia, glaucoma, intellectual disability syndrome 733455003 Spastic paraplegia, severe developmental delay, epilepsy syndrome 1187278006 SPOAN and SPOAN-related disorder 789674008 X-linked complex hereditary spastic paraplegia 1156841003 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Spastic syndrome 386781001 Spastic paraplegia 192967009 Hereditary spastic paraplegia 39912006 Complicated hereditary spastic paraplegia 230261006 ancestors sorted most to least specific
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