718103001: Hereditary geniospasm (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of movement\Movement disorder\Hereditary geniospasm
• \General finding of soft tissue\Peripheral nerve finding\Peripheral neuropathy\Disorder of facial nerve\Hereditary geniospasm
• \General finding of soft tissue\Disorder of soft tissue\Peripheral neuropathy\Disorder of facial nerve\Hereditary geniospasm
• \Finding of head and neck region\Disorder of facial nerve\Hereditary geniospasm
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary geniospasm
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary geniospasm
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary geniospasm
• \Disease\Disorder of body system\Neurological disorder\Neuropathy\Peripheral neuropathy\Disorder of facial nerve\Hereditary geniospasm
• \Disease\Disorder of body system\Neurological disorder\Neuropathy\Disorder of cranial nerve\Disorder of facial nerve\Hereditary geniospasm
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary geniospasm
• \Disease\Disorder of body system\Neurological disorder\Disorder of the peripheral nervous system\Peripheral neuropathy\Disorder of facial nerve\Hereditary geniospasm
• \Disease\Movement disorder\Hereditary geniospasm
• \Disease\Disorder of soft tissue\Peripheral neuropathy\Disorder of facial nerve\Hereditary geniospasm

Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3310457019	Hereditary geniospasm (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3310458012	Hereditary geniospasm	en	Synonym	Active	Case insensitive	SNOMED CT core
3311096010	Familial trembling of chin	en	Synonym	Active	Case insensitive	SNOMED CT core
3311180014	Hereditary chin trembling	en	Synonym	Active	Case insensitive	SNOMED CT core
3311181013	A movement disorder with manifestation of episodes of involuntary tremor of the chin and lower lip. The disorder has been described in less than 25 families from Europe and the USA, with a slight male preponderance. Onset usually occurs in childhood and may be precipitated by stress and emotion. Episodes may occur during sleep. There are no associated neurological abnormalities. Spontaneous improvement with age is possible. Inheritance is autosomal dominant.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Queensland allied health clinical finding reference set

Queensland allied health indicator for intervention reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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