763624007: Syndactyly type 6 (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of limb structure\Disorder of extremity\...
• \Disorder of digit\Congenital anomaly of digit\Syndactyly\Syndactyly type 6
• \Congenital anomaly of limb\Congenital anomaly of digit\Syndactyly\Syndactyly type 6
• \Disease\Disorder of extremity\Disorder of digit\Congenital anomaly of digit\Syndactyly\Syndactyly type 6
• \Disease\Disorder of extremity\Congenital anomaly of limb\Congenital anomaly of digit\Syndactyly\Syndactyly type 6
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of limb\Congenital anomaly of digit\Syndactyly\Syndactyly type 6
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of limb\Congenital anomaly of digit\Syndactyly\Syndactyly type 6

Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3643074013	Syndactyly type 6	en	Synonym	Active	Case insensitive	SNOMED CT core
3643075014	Syndactyly type 6 (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3643076010	Syndactyly mitten type	en	Synonym	Active	Case insensitive	SNOMED CT core
3643077018	A rare genetic non-syndromic congenital limb malformation with characteristics of unilateral fusion of second to fifth fingers, amalgamation of distal phalanges in a knot-like structure, and second and third-toe fusion. Some individuals present only with webbing between second and third toes without involvement of fingers.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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