Cytoscape Web
Click node...


1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hydranencephaly
Lissencephaly due to LIS1 mutation

NDE1 PAFAH1B1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NDE1
(0.86)
PAFAH1B1



Citations in the biomedical literature:


Hydranencephaly
NDE1
Lissencephaly due to LIS1 mutation
PAFAH1B1



Hydranencephaly
Lissencephaly due to LIS1 mutation

Synonym(s):
(no synonyms)

Synonym(s):
- PAFAH1B1-associated lissencephaly

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):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
No OMIM references
1 MeSH reference: D006832
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.