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Congenital anomaly of cerebrum 702628006 SNOMED CT code SNOMED code 702628006 name Congenital anomaly of cerebrum status active date introduced 2014-07-31 fully specified name(s) Congenital anomaly of cerebrum (disorder) synonyms Congenital anomaly of cerebrum attributes - group1 Associated morphology Morphologically abnormal structure 49755003 Pathological process Pathological developmental process 308490002 Finding site Cerebrum 83678007 Occurrence Congenital 255399007 parents Congenital anomaly of brain 57148006 children Absence of septum pellucidum 253143001 Agenesis of cerebrum 204040004 Alobar holoprosencephaly 253137003 Anomalies of hypothalamus 204046005 Aprosencephaly/atelencephaly spectrum 1237365009 Bilateral frontal polymicrogyria 890285006 Bilateral frontoparietal polymicrogyria 890286007 Bilateral generalized polymicrogyria 890287003 Bilateral parasagittal parieto-occipital polymicrogyria 890288008 CEDNIK syndrome 722385008 Cerebral cortical dysgenesis 31429000 Colpocephaly 253160006 Congenital abnormal shape of cerebrum 92905000 Congenital achiasma 734031008 Congenital anomaly of pituitary gland 74012004 Congenital hypoplasia of cerebrum 93249003 Congenital malformation of corpus callosum 204042007 Congenital porencephalic cyst 330041000119103 Cortical dysplasia 253153000 Craniosynostosis and intracranial calcification syndrome 720816004 Cystic leukoencephalopathy without megalencephaly 720825005 Defect of telencephalic division 253135006 Diencephalic mesencephalic junction dysplasia 766871009 Ectopic gray matter in centrum ovale 54794009 Encephalopathy, intracerebral calcification, retinal degeneration syndrome 733049004 Endocrine-cerebro-osteodysplasia syndrome 723309006 Epileptic encephalopathy with global cerebral demyelination 726702005 Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome 782754006 Hemispheric cerebral agenesis 56155002 Hydranencephaly 30023002 Isolated arhinencephaly 771147003 Keratosis follicularis, dwarfism, cerebral atrophy syndrome 723830005 Kundrat's syndrome 30278004 Lissencephaly due to LIS1 mutation 770560008 Lobar holoprosencephaly 253136007 Macroencephaly 9740002 Macrogyria 23024003 Microcephalic cortical malformations, short stature due to RTTN deficiency 1187195007 Microdysgenesis 253167009 Middle interhemispheric variant of holoprosencephaly 866053004 Partial absence of septum pellucidum 422474003 Polymicrogyria due to TUBB2B mutation 1208935007 Schizencephaly 253159001 Semi-lobar holoprosencephaly 253138008 Status marmoratus 62158001 Subcortical nodular heterotopia 1010663004 Tubulinopathy-associated dysgyria 1187215002 Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome 719833004 Worster Drought syndrome 716335003 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 246556002 23853001 128124001 57148006 702628006 ancestors sorted most to least specific
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