Craniosynostosis syndrome 57219006 SNOMED CT code SNOMED code 57219006 name Craniosynostosis syndrome status active date introduced 2002-01-31 fully specified name(s) Craniosynostosis syndrome (disorder) synonyms CSO - Craniosynostosis Premature cranial suture closure Craniosynostosis syndrome Craniostosis Craniosynostosis Premature closure of cranial sutures Congenital ossification of cranial sutures Congenital ossification of sutures of skull Craniostenosis attributes - group1 Occurrence Congenital 255399007 Pathological process Pathological developmental process 308490002 Associated morphology Congenital premature fusion 67798003 Finding site Joint structure of suture of skull 51863000 parents Imperfect fusion of skull 23939000 children Acrobrachycephaly 711039004 Acrocephalosyndactyly 268262006 Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome 722281001 Antley-Bixler syndrome 62964007 Baller-Gerold syndrome 77608001 Bicoronal craniosynostosis 254021002 Capra DeMarco syndrome 720815000 Cardiocranial syndrome Pfeiffer type 720606005 Complex craniosynostosis 8611000119100 Craniofacial dyssynostosis syndrome 720755009 Craniofrontonasal dysplasia with Poland anomaly syndrome 720757001 Craniomicromelic syndrome 725098001 Craniorhiny 784350004 Craniosynostosis and dental anomalies syndrome 773332008 Craniosynostosis and intracranial calcification syndrome 720816004 Craniosynostosis Boston type 720817008 Craniosynostosis fibular aplasia syndrome 732250002 Craniosynostosis Herrmann Opitz type 763684005 Craniosynostosis Philadelphia type 720818003 Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome 720813007 Craniosynostosis, anal anomaly, porokeratosis syndrome 720812002 Craniosynostosis, microretrognathia, severe intellectual disability syndrome 1269224009 Crouzon syndrome 28861008 Curry Jones syndrome 720819006 Cutis gyrata syndrome of Beare and Stevenson 703528008 FGFR2-related bent bone dysplasia 778008009 Fibroblast growth factor receptor 3-related craniosynostosis 440350001 Holoprosencephaly craniosynostosis syndrome 715434005 Hunter McAlpine craniosynostosis syndrome 721227001 Lethal occipital encephalocele, skeletal dysplasia syndrome 773672007 Long narrow head 72239002 Lowry MacLean syndrome 721974000 Metopic ridging, ptosis, facial dysmorphism syndrome 1179283004 Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome 722051004 Pseudoaminopterin syndrome 715867000 SCARF syndrome 734173003 Schprintzen 277945007 removed: 2017-07-31 Shprintzen Goldberg craniosynostosis syndrome 719069008 Simple craniosynostosis 255581000119100 Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome 718766002 Trigonocephaly 28740008 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 106028002 118952005 248387005 23939000 57219006 ancestors sorted most to least specific
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