703508009: Ear, patella, short stature syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of general physiological development\Disorder of stature\Short stature disorder\Primordial dwarfism\Ear, patella, short stature syndrome
• \General finding of observation of patient\Body measurement finding\Height / growth finding\General finding of height\Disorder of stature\Short stature disorder\Primordial dwarfism\Ear, patella, short stature syndrome
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Ear, patella, short stature syndrome
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Ear, patella, short stature syndrome
• \Disease\Developmental disorder\Developmental hereditary disorder\Ear, patella, short stature syndrome
• \Disease\Developmental disorder\Disorder of stature\Short stature disorder\Primordial dwarfism\Ear, patella, short stature syndrome

Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3008731011	Microtia, absent patellae, micrognathia syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3008783016	Ear, patella, short stature syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3008797012	Meier-Gorlin syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3008846014	Ear, patella, short stature syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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