232059000: Laurence-Moon syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Mental state, behaviour and/or psychosocial function finding\Behaviour finding\Intellectual disability\Laurence-Moon syndrome
• \Functional finding\Cognitive function finding\Impaired cognition\Intellectual disability\Laurence-Moon syndrome
• \Functional finding\Cognitive function finding\Intellectual ability - finding\Intellectual disability\Laurence-Moon syndrome
• \Functional finding\Intelligence finding\Intellectual ability - finding\Intellectual disability\Laurence-Moon syndrome
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Laurence-Moon syndrome
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Laurence-Moon syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Laurence-Moon syndrome
• \Disease\Developmental disorder\Neurodevelopmental disorder\Intellectual disability\Laurence-Moon syndrome
• \Disease\Developmental disorder\Developmental hereditary disorder\Laurence-Moon syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Laurence-Moon syndrome

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
347710015	Laurence-Moon syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
620075014	Laurence-Moon 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

Australian dialect reference set

Problem/Diagnosis reference set

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