ODCs

Click node...

1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Charcot-Marie-Tooth disease type 1A

Acute inflammatory demyelinating polyradiculoneuropathy

Citations in the biomedical literature:

Charcot-Marie-Tooth disease type 1A		Acute inflammatory demyelinating polyradiculoneuropathy
	Synonym(s): - CMT1A - Microduplication 17p12		Synonym(s): - AIDP - Acute idiopathic demyelinating polyneuropathy - Acute inflammatory polyneuropathy - GBS, acute inflammatory demyelinating polyradiculoneuropathic form - Guillain-BarrÃ© syndrome, acute inflammatory demyelinating polyradiculoneuropathic form

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: variable Average age of death: any age Type of inheritance: multigenic/multifactorial

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.