medcodeid term originalreadcode cleansedreadcode snomedctconceptid SnomedCTDescriptionId release emiscodecategoryid 72531016 congenital hemiplegia F231 F231.00 1593000 3769017 32 2524111000006113 postnatal infantile hemiplegia ^ESCTPO252411 1593000 3770016 32 297232013 infantile hemiplegia nos F234 F234.00 1593000 3769017 32 254829017 o/e - hemiplegia 2833 2833.00 163601006 254829017 27 4566571000006117 on examination - hemiplegia ^ESCTON456657 163601006 2666566016 27 4566621000006119 on examination - paraplegia ^ESCTON456662 163604003 2666568015 27 254833012 o/e - paraplegia 2835 2835.00 163604003 254833012 27 223801000000115 paraplegia - congenital F230-1 F230.11 192949002 297221013 32 297221013 congenital paraplegia F2300 F230000 192949002 297221013 32 297243017 flaccid paraplegia F2410 F241000 192966000 297243017 32 297244011 spastic paraplegia F2411 F241100 192967009 297244011 32 415146010 right hemiplegia F223 F223.00 278284007 415146010 32 415147018 left hemiplegia F222 F222.00 278285008 415147018 32 5611491000006112 lt - left hemiplegia ^ESCTLT561149 278285008 415148011 32 66483014 hereditary spastic paraplegia F141 F141.00 39912006 66483014 32 3142321000006114 familial spastic paraplegia syndrome ^ESCTFA314232 39912006 66485019 32 3142311000006118 strumpell-lorrain disease ^ESCTST314231 39912006 66484015 32 3142351000006117 spastic congenital paraplegia ^ESCTSP314235 39912006 2477033013 32 3142341000006119 strumpell disease ^ESCTST314234 39912006 1229577015 32 3142331000006112 hsp - hereditary spastic paraplegia ^ESCTHS314233 39912006 1229576012 32 84272011 hemiplegia F22 F22..00 50582007 84272011 32 297210016 hemiplegia nos F22z F22z.00 50582007 84272011 32 3319161000006112 hemiplegia (paralysis on one side) ^ESCTHE331916 50582007 2966634017 32 3480751000006110 paralysis of both lower limbs ^ESCTPA348075 60389000 100324017 32 3480771000006117 paraplegia (complete or partial paralysis of legs) ^ESCTPA348077 60389000 2966653010 32 3480761000006112 lower paraplegia ^ESCTLO348076 60389000 100325016 32 100323011 paraplegia F241 F241.00 60389000 100323011 32 494103012 tropical spastic paraplegia F038 F038.00 714279000 3299127017 32 7717301000006113 htlv-i-associated myelopathy ^ESCTHT771730 714279000 3299399016 32 7717321000006115 myelopathy caused by human t-lymphotropic virus 1 ^ESCTMY771732 714279000 3299925012 32 7717311000006111 tropical spastic paraparesis ^ESCTTR771731 714279000 3299597018 32 7717281000006114 human t-cell lymphotropic virus 1-associated myelopathy ^ESCTHU771728 714279000 3299711016 32 132112014 spastic hemiplegia F221 F221.00 79633009 132112014 32 134251013 flaccid hemiplegia F220 F220.00 80935004 134251013 32 3845841000006114 fibrodysplasia ossificans progressiva ^ESCTFI384584 82725007 1234729013 32 3845871000006118 myositis ossificans progressiva ^ESCTMY384587 82725007 3036461013 32 3845851000006111 fop - fibrodysplasia ossificans progressiva ^ESCTFO384585 82725007 1234730015 32 3845831000006116 diffuse progressive ossifying polymyositis ^ESCTDI384583 82725007 137235014 32 137233019 progressive myositis ossificans N2311 N231100 82725007 137233019 32 716831000006114 massive muscular calcification associated with paraplegia N2310-1 N231011 82725007 3036461013 32 3845821000006119 mãƒâ¼nchmeyer disease ^ESCTMÃœ384582 82725007 137234013 32 1234731016 fibrodysplasia ossificans congenita PGy4 PGy4.00 82725007 1234731016 32 856091000006114 right hemiplegia EGTONRI2 856091000006105 856091000006114 32 857181000006110 left hemiplegia EGTONLE2 857181000006106 857181000006110 27 905891000006114 [rfc] paraplegias HNG0058 905891000006105 905891000006114 12