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Lissencephaly due to TUBA1A mutation
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Muscle-eye-brain disease with bilateral multicystic leucodystrophy
1 associated gene
No signs/symptoms info
Lissencephaly due to TUBA1A mutation
Muscle-eye-brain disease with bilateral multicystic leucodystrophy

TUBA1A
(UniProt - OMIM)
 DAG1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TUBA1A
(0.75)
DAG1


Citations in the biomedical literature:


Lissencephaly due to TUBA1A mutation
TUBA1A
Muscle-eye-brain disease with bilateral multicystic leucodystrophy
DAG1



Lissencephaly due to TUBA1A mutation
Muscle-eye-brain disease with bilateral multicystic leucodystrophy

Synonym(s):
(no synonyms)

Synonym(s):
- MEB disease with bilateral multicystic leucodystrophy
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -
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.