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

Charcot-Marie-Tooth disease type 1E


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

Citations in the biomedical literature:

Dejerine-Sottas syndrome		Charcot-Marie-Tooth disease type 1E
	Synonym(s): - Charcot-Marie-Tooth disease type 3 - HMSN 3 - Hereditary motor and sensory neuropathy type 3 - Hypertrophic neuropathy of infancy		Synonym(s): - CMT1E - Charcot-Marie-Tooth disease - deafness

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease - Rare otorhinolaryngologic 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: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: C538392		External references: 1 OMIM reference - 2 MeSH references: C537986 / C538078

No signs/symptoms info available.