719158007: Syndactyly type 4 (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of limb structure\Disorder of extremity\...
• \Disorder of digit\Congenital anomaly of digit\Syndactyly\Syndactyly type 4
• \Congenital anomaly of limb\Congenital anomaly of digit\Syndactyly\Syndactyly type 4
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Syndactyly type 4
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Syndactyly type 4
• \Disease\Disorder of extremity\Disorder of digit\Congenital anomaly of digit\Syndactyly\Syndactyly type 4
• \Disease\Disorder of extremity\Congenital anomaly of limb\Congenital anomaly of digit\Syndactyly\Syndactyly type 4
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of limb\Congenital anomaly of digit\Syndactyly\Syndactyly type 4
• \Disease\Developmental disorder\Developmental hereditary disorder\Syndactyly type 4
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of limb\Congenital anomaly of digit\Syndactyly\Syndactyly type 4

Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3315199014	Syndactyly type 4 (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3315200012	Syndactyly type 4	en	Synonym	Active	Case insensitive	SNOMED CT core
3315201011	Haas type syndactyly	en	Synonym	Active	Case sensitive	SNOMED CT core
3315202016	A very rare congenital distal limb malformation with characteristics of complete bilateral syndactyly involving all digits 1 to 5. So far, only four reports have been described in the literature. A frequent association with polydactyly (with six metacarpals and six digits) has been reported. Feet are affected occasionally. The SD4 locus maps to 7q36. The condition is inherited as an autosomal dominant trait.	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

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