Cytoscape Web
Click node...

Autosomal recessive spastic paraplegia type 58
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Distal 17p13.3 microdeletion syndrome
1 associated gene
No signs/symptoms info
Autosomal recessive spastic paraplegia type 58
Distal 17p13.3 microdeletion syndrome

KIF1C
(UniProt - OMIM)
 YWHAE
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
KIF1C
(0.85)
YWHAE


Citations in the biomedical literature:


Autosomal recessive spastic paraplegia type 58
KIF1C
Distal 17p13.3 microdeletion syndrome
YWHAE



Autosomal recessive spastic paraplegia type 58
Distal 17p13.3 microdeletion syndrome

Synonym(s):
- SPG58
Synonym(s):
- Distal del(17)(p13.3 )
- Distal monosomy 17p13.3
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.