ODCs

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

PROTEIN INTERACTIONS: 1

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

Dejerine-Sottas syndrome

Autosomal recessive limb-girdle muscular dystrophy type 2P


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PRX	(0.72)	DAG1

Citations in the biomedical literature:

Dejerine-Sottas syndrome		Autosomal recessive limb-girdle muscular dystrophy type 2P
	Synonym(s): - Charcot-Marie-Tooth disease type 3 - HMSN 3 - Hereditary motor and sensory neuropathy type 3 - Hypertrophic neuropathy of infancy		Synonym(s): - LGMD2P

	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: Class of prevalence: - Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.