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

Hemolytic anemia due to diphosphoglycerate mutase deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EGR2	(0.63)	BPGM

Citations in the biomedical literature:

Dejerine-Sottas syndrome		Hemolytic anemia due to diphosphoglycerate mutase deficiency
	Synonym(s): - Charcot-Marie-Tooth disease type 3 - HMSN 3 - Hereditary motor and sensory neuropathy type 3 - Hypertrophic neuropathy of infancy		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare hematologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	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 - No MeSH references

No signs/symptoms info available.