205800003: Gorlin-Chaudhry-Moss syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Developmental hereditary disorder\Gorlin-Chaudhry-Moss syndrome
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Gorlin-Chaudhry-Moss syndrome
• \Congenital disease\Congenital anomaly\Congenital malformation syndrome\Gorlin-Chaudhry-Moss syndrome
• \Developmental disorder\Developmental hereditary disorder\Gorlin-Chaudhry-Moss syndrome
• \Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Gorlin-Chaudhry-Moss syndrome

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

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

Back to Start