205800003: Gorlin-Chaudhry-Moss syndrome (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Genetic disease\Hereditary disease\...
• \Developmental hereditary disorder\Gorlin-Chaudhry-Moss syndrome
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Gorlin-Chaudhry-Moss syndrome
• \Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital malformation\Congenital malformation syndrome (disorder)\Gorlin-Chaudhry-Moss syndrome
• \Developmental disorder\Developmental hereditary disorder\Gorlin-Chaudhry-Moss syndrome
• \Developmental disorder\Congenital malformation\Congenital malformation syndrome (disorder)\Gorlin-Chaudhry-Moss syndrome

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
315590011	Gorlin-Chaudhry-Moss syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
591218010	Gorlin-Chaudhry-Moss syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

Back to Start