718222000: Autosomal dominant popliteal pterygium syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of limb structure\Disorder of extremity\Disorder of lower extremity\Disorder of free lower limb\Disorder of knee\Popliteal pterygium syndrome\Autosomal dominant popliteal pterygium syndrome
• \Finding of limb structure\Disorder of extremity\Disorder of lower extremity\Congenital anomaly of lower limb\Popliteal pterygium syndrome\Autosomal dominant popliteal pterygium syndrome
• \Finding of limb structure\Disorder of extremity\Congenital anomaly of limb\Congenital anomaly of lower limb\Popliteal pterygium syndrome\Autosomal dominant popliteal pterygium syndrome
• \Finding of limb structure\Finding of lower limb\Disorder of lower extremity\Disorder of free lower limb\Disorder of knee\Popliteal pterygium syndrome\Autosomal dominant popliteal pterygium syndrome
• \Finding of limb structure\Finding of lower limb\Disorder of lower extremity\Congenital anomaly of lower limb\Popliteal pterygium syndrome\Autosomal dominant popliteal pterygium syndrome
• \Finding of limb structure\Finding of lower limb\Finding of knee region\Disorder of knee\Popliteal pterygium syndrome\Autosomal dominant popliteal pterygium syndrome
• \Disease\Disorder of joint region\Disorder of knee\Popliteal pterygium syndrome\Autosomal dominant popliteal pterygium syndrome
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Autosomal dominant popliteal pterygium syndrome
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant popliteal pterygium syndrome
• \Disease\Disorder of extremity\Disorder of lower extremity\Disorder of free lower limb\Disorder of knee\Popliteal pterygium syndrome\Autosomal dominant popliteal pterygium syndrome
• \Disease\Disorder of extremity\Disorder of lower extremity\Congenital anomaly of lower limb\Popliteal pterygium syndrome\Autosomal dominant popliteal pterygium syndrome
• \Disease\Disorder of extremity\Congenital anomaly of limb\Congenital anomaly of lower limb\Popliteal pterygium syndrome\Autosomal dominant popliteal pterygium syndrome
• \Disease\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with limb defect as major feature\Popliteal pterygium syndrome\Autosomal dominant popliteal pterygium syndrome
• \Disease\Congenital disease\Congenital malformation\Congenital abnormality of lower limb and pelvic girdle\Congenital anomaly of lower limb\Popliteal pterygium syndrome\Autosomal dominant popliteal pterygium syndrome
• \Disease\Congenital disease\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of lower limb\Popliteal pterygium syndrome\Autosomal dominant popliteal pterygium syndrome
• \Disease\Developmental disorder\Developmental hereditary disorder\Autosomal dominant popliteal pterygium syndrome
• \Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with limb defect as major feature\Popliteal pterygium syndrome\Autosomal dominant popliteal pterygium syndrome
• \Disease\Developmental disorder\Congenital malformation\Congenital abnormality of lower limb and pelvic girdle\Congenital anomaly of lower limb\Popliteal pterygium syndrome\Autosomal dominant popliteal pterygium syndrome
• \Disease\Developmental disorder\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of lower limb\Popliteal pterygium syndrome\Autosomal dominant popliteal pterygium syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3311572010	Autosomal dominant popliteal pterygium syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3311573017	Autosomal dominant popliteal pterygium syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3311574011	Facio-genito-popliteal syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3311575012	Popliteal web syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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