Monosomy and deletion from autosome 205627002 SNOMED CT code SNOMED code 205627002 name Monosomy and deletion from autosome status active date introduced 2002-01-31 fully specified name(s) Monosomy and deletion from autosome (disorder) synonyms Monosomy and deletion from autosome Monosomies and deletions from the autosomes attributes - group1 Occurrence Congenital 255399007 Associated morphology Cellular AND/OR subcellular abnormality 107673000 Finding site Chromosome 91272006 parents Anomaly of chromosome pair 362984008 children [X]Other deletions from the autosomes 205990009 removed: 2009-01-31 Antimongolism syndrome 205628007 removed: 2009-07-31 Autosomal deletion - mosaicism 254273005 Complete monosomy of autosome 726364006 Deletion of part of autosome 254274004 Deletion seen only at prometaphase 205634000 Deletion with complex rearrangement 274908005 Monosomy 21, mosaicism 205638002 Whole chromosome monosomy - meiotic nondisjunction 205636003 Whole chromosome monosomy - mitotic nondisjunction mosaicism 270520003 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Monosomy and deletion from autosome 205627002 ancestors sorted most to least specific
cpt crosswalks Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.
Access to this feature is available in the following products:CPT® to SNOMED Crosswalks sign IN sign UP
Thank you for choosing Find-A-Code, please Sign In to remove ads.