ODCs

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1 OMIM reference -
4 associated genes
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

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

Dejerine-Sottas syndrome

Acute inflammatory demyelinating polyradiculoneuropathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MPZ	(0.94)	PMP22

Citations in the biomedical literature:

Dejerine-Sottas syndrome		Acute inflammatory demyelinating polyradiculoneuropathy
	Synonym(s): - Charcot-Marie-Tooth disease type 3 - HMSN 3 - Hereditary motor and sensory neuropathy type 3 - Hypertrophic neuropathy of infancy		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 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: - Average age onset: neonatal/infancy 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 - 1 MeSH reference: C538392		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.