ODCs

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1 OMIM reference -
2 associated genes
6 signs/symptoms

COMMON GENES: 2
PROTEIN INTERACTIONS: 1

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

Roussy-LÃ©vy syndrome

Dejerine-Sottas syndrome


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

Citations in the biomedical literature:

Roussy-LÃ©vy syndrome		Dejerine-Sottas syndrome
	Synonym(s): - Hereditary areflexic dystasia, Roussy-LÃ©vy type		Synonym(s): - Charcot-Marie-Tooth disease type 3 - HMSN 3 - Hereditary motor and sensory neuropathy type 3 - Hypertrophic neuropathy of infancy

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: - Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C538392

Roussy-LÃ©vy syndrome
	Very frequent - Abnormal gait - Areflexia / hyporeflexia - Autosomal recessive inheritance - Movement disorder - Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy - Nerve conduction abnormality
Dejerine-Sottas syndrome
(no data available)