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Thyroxine transport defect 56112001 SNOMED CT code SNOMED code 56112001 name Thyroxine transport defect status active date introduced 2002-01-31 fully specified name(s) Thyroxine transport defect (disorder) synonyms Thyroxine transport defect attributes - group1 Occurrence Congenital 255399007 Finding site Thyroid structure 69748006 parents Inherited disorder of thyroid metabolism 36985004 children Autosomal dominant excess of transthyretin 66185005 Autosomal dominant variant form of albumin 21367009 Thyroxine plasma membrane transport defect 79488001 X-linked absence of thyroxine-binding globulin 2241003 X-linked excess of thyroxine-binding globulin 55296004 X-linked reduction of thyroxine-binding globulin 41300001 X-linked variant form of thyroxine-binding globulin 73068003 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of neck 118939000 Disorder of thyroid gland 14304000 Inherited disorder of thyroid metabolism 36985004 Thyroxine transport defect 56112001 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.
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