ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

3 OMIM references -
2 associated genes
No signs/symptoms info

Lissencephaly due to LIS1 mutation

Subcortical band heterotopia

PAFAH1B1	(UniProt - OMIM)		DCX	(UniProt - OMIM)
			PAFAH1B1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PAFAH1B1	(0.88)	DCX

Citations in the biomedical literature:

Lissencephaly due to LIS1 mutation		Subcortical band heterotopia
	Synonym(s): - PAFAH1B1-associated lissencephaly		Synonym(s): - Subcortical laminar heterotopia

	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: 1 OMIM reference - No MeSH references		External references: 3 OMIM references - No MeSH references

No signs/symptoms info available.