ODCs

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

COMMON GENES: 1

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

Pelizaeus-Merzbacher-like due to GJC2 mutation

Autosomal recessive spastic paraplegia type 44

GJC2

Citations in the biomedical literature:

Pelizaeus-Merzbacher-like due to GJC2 mutation		Autosomal recessive spastic paraplegia type 44
	Synonym(s): - PMLD1		Synonym(s): - SPG44

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

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Diseases of the nervous system -

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

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

No signs/symptoms info available.