ODCs

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1 OMIM reference -
2 associated genes
6 signs/symptoms

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

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

Roussy-LÃ©vy syndrome

Autosomal dominant Charcot-Marie-Tooth disease type 2I

MPZ	(UniProt - OMIM)		MPZ	(UniProt - OMIM)
PMP22	(UniProt - OMIM)


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

Citations in the biomedical literature:

Roussy-LÃ©vy syndrome		Autosomal dominant Charcot-Marie-Tooth disease type 2I
	Synonym(s): - Hereditary areflexic dystasia, Roussy-LÃ©vy type		Synonym(s): - CMT2I

	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: adulthood Average age of death: - Type of inheritance: autosomal dominant

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

Roussy-LÃ©vy syndrome
	Very frequent - Abnormal gait - Areflexia / hyporeflexia - Autosomal recessive inheritance - Movement disorder - Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy - Nerve conduction abnormality
Autosomal dominant Charcot-Marie-Tooth disease type 2I
(no data available)