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Roussy-Lévy syndrome
1 OMIM reference -
2 associated genes
22 connected diseases
6 signs/symptoms
Disease Type of connection
Dejerine-Sottas syndrome
Acute inflammatory demyelinating polyradiculoneuropathy
Autosomal dominant Charcot-Marie-Tooth disease type 2I
Autosomal dominant Charcot-Marie-Tooth disease type 2J
Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
Charcot-Marie-Tooth disease type 1A
Charcot-Marie-Tooth disease type 1B
Charcot-Marie-Tooth disease type 1E
Hereditary neuropathy with liability to pressure palsies
Infantile Refsum disease
Neonatal adrenoleukodystrophy
Zellweger syndrome
Alternating hemiplegia of childhood
Atelosteogenesis type I
Atelosteogenesis type III
Autosomal dominant Larsen syndrome
Boomerang dysplasia
Distal myopathy with posterior leg and anterior hand involvement
Familial or sporadic hemiplegic migraine
Muscle filaminopathy
Spondylocarpotarsal synostosis
Synonym(s):
- Hereditary areflexic dystasia, Roussy-Lévy type
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
MPZ P25189159440
PMP22 Q01453601097
Very frequent
- Abnormal gait
- Areflexia / hyporeflexia
- Autosomal recessive inheritance
- Movement disorder
- Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy
- Nerve conduction abnormality