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Congenital anomaly of nervous system 88425004 SNOMED CT code SNOMED code 88425004 name Congenital anomaly of nervous system status active date introduced 2002-01-31 fully specified name(s) Congenital anomaly of nervous system (disorder) synonyms Congenital anomaly of nervous system Congenital disease of nervous system Congenital lesion of nervous system Congenital deformity of nervous system Congenital malformation of the nervous system attributes - group1 Associated morphology Morphologically abnormal structure 49755003 Pathological process Pathological developmental process 308490002 Occurrence Congenital 255399007 Finding site Nervous system structure 25087005 parents children [X]Congenital malformations of the nervous system 205845004 removed: 2009-01-31 [X]Other specified congenital malformations of brain 205849005 removed: 2009-01-31 [X]Other specified congenital malformations of nervous system 205853007 removed: 2009-01-31 Abnormality of neurogenesis 253128003 Agenesis of nerve 111338006 Angelman syndrome 76880004 Cerebro-oculo-facio-skeletal syndrome 41283003 Congenital anomaly of central nervous system 128124001 Congenital anomaly of nervous system of head/neck 287080001 Congenital anomaly of neural structure of trunk 363034005 Congenital anomaly of the peripheral nervous system 22133005 Congenital anosmia 230502003 Congenital CNS anomalies NOS 268309002 removed: 2010-01-31 Congenital degeneration of nervous system 95477007 Congenital flaccid paralysis 95652003 Congenital hypomyelinating neuropathy 230562000 Congenital malformation of autonomic nervous system 722996009 De Lange syndrome 40354009 Dysmorphic sialidosis, congenital form 27642008 Ecchordosis physaliphora 69664005 Ectopic gray matter 266673001 Fibrous skin tumor of tuberous sclerosis 36025004 Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome 733469003 Hereditary neurocutaneous angiomata 403775003 HIVEP2-related intellectual disability 765434008 Hypogonadism with anosmia 93559003 Hypomyelination neuropathy arthrogryposis syndrome 766931003 Male emopamil-binding protein disorder with neurological defect 782739000 Nervous system anomalies NOS 204097002 removed: 2010-01-31 Neural tube defect 253098009 Neuroectodermal melanolysosomal disease 724091002 Neuronal choristoma 230794008 Other nervous system congenital anomalies 204018008 removed: 2010-01-31 Other specified brain anomalies 204066001 removed: 2010-01-31 Other specified nervous system anomalies 204084004 removed: 2010-01-31 Papular epidermal nevi with skyline basal cell layers syndrome 771473004 Proteus syndrome 23150001 Pulmonary tuberous sclerosis 233718008 Sotos' syndrome 75968004 Unspecified nervous system anomaly of brain, cord and nervous system 204093003 removed: 2010-01-31 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 64572001 362965005 118940003 88425004 138875005 404684003 64572001 5294002 276654001 88425004 ancestors sorted most to least specific
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