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Autosomal recessive spastic paraplegia type 58
1 OMIM reference -
1 associated gene
4 connected diseases
No signs/symptoms info
Disease Type of connection
17p13.3 microduplication syndrome
Distal 17p13.3 microdeletion syndrome
Miller-Dieker syndrome
Occipital pachygyria and polymicrogyria
Synonym(s):
- SPG58
Classification (Orphanet):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
KIF1C O43896603060
No signs/symptoms info available.