718880003: Zellweger-like syndrome without peroxisomal anomaly (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Developmental hereditary disorder\Zellweger-like syndrome without peroxisomal anomaly
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Zellweger-like syndrome without peroxisomal anomaly
• \Metabolic disease\Mitochondrial cytopathy\Zellweger-like syndrome without peroxisomal anomaly
• \Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with unusual brain and/or neuromuscular findings\Zellweger-like syndrome without peroxisomal anomaly
• \Developmental disorder\Developmental hereditary disorder\Zellweger-like syndrome without peroxisomal anomaly
• \Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with unusual brain and/or neuromuscular findings\Zellweger-like syndrome without peroxisomal anomaly

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3314289019	Zellweger-like syndrome without peroxisomal anomaly (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
3314290011	Zellweger-like syndrome without peroxisomal anomaly	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3314291010	Ahn Lerman Sagie syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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