Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Lissencephaly due to TUBA1A mutation
Melanoma and neural system tumor syndrome

TUBA1A CDKN2A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TUBA1A
(0.68)
CDKN2A



Citations in the biomedical literature:


Lissencephaly due to TUBA1A mutation
TUBA1A
Melanoma and neural system tumor syndrome
CDKN2A



Lissencephaly due to TUBA1A mutation
Melanoma and neural system tumor syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- Melanoma-astrocytoma syndrome

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare neurologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
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.