726629006: Scalp defect postaxial polydactyly syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Developmental hereditary disorder\Scalp defect postaxial polydactyly syndrome
• \Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Scalp defect postaxial polydactyly syndrome
• \Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Scalp defect postaxial polydactyly syndrome
• \Developmental disorder\Developmental hereditary disorder\Scalp defect postaxial polydactyly syndrome
• \Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Scalp defect postaxial polydactyly syndrome

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3451116010	Scalp defect postaxial polydactyly syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3451117018	Scalp defect postaxial polydactyly syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3451118011	Syndrome with characteristics of congenital scalp defects and postaxial polydactyly type A. It is an extremely rare condition. The syndrome has variable manifestations with one affected person with both congenital scalp defects and postaxial polydactyly type A, 4 people with scalp defects only and 3 people who had postaxial polydactyly only. Transmission is autosomal dominant.	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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