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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
29 OMIM references -
16 associated genes
No signs/symptoms info
Autosomal dominant spastic paraplegia type 8
Autosomal recessive nonsyndromic intellectual deficit

KIAA0196 CC2D1A
CRADD
CRBN
GRIK2
KIAA1033
LINS
MAN1B1
MED13L
MED23
NSUN2
PRSS12
ST3GAL3
TECR
TRAPPC9
TUSC3
ZC3H14


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KIAA0196
(0.83)
KIAA1033



Citations in the biomedical literature:


Autosomal dominant spastic paraplegia type 8
KIAA0196
Autosomal recessive nonsyndromic intellectual deficit
CC2D1A CRADD CRBN GRIK2 KIAA1033 LINS
MAN1B1 MED13L MED23 NSUN2 PRSS12 ST3GAL3
TECR TRAPPC9 TUSC3 ZC3H14



Autosomal dominant spastic paraplegia type 8
Autosomal recessive nonsyndromic intellectual deficit

Synonym(s):
- SPG8

Synonym(s):
- NS-ARID

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
1 MeSH reference: C536867
External references:
29 OMIM references -
No MeSH references

No signs/symptoms info available.