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Autosomal recessive spastic paraplegia type 44
1 OMIM reference -
1 associated gene
3 connected diseases
No signs/symptoms info
Disease Type of connection
Milroy disease
Pelizaeus-Merzbacher-like due to GJC2 mutation
Congenital analbuminemia
Synonym(s):
- SPG44
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
GJC2 Q5T442608803
No signs/symptoms info available.