ODCs

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

PROTEIN INTERACTIONS: 1

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

Periventricular nodular heterotopia

Combined immunodeficiency due to STK4 deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLNA	(0.63)	STK4

Citations in the biomedical literature:

Periventricular nodular heterotopia		Combined immunodeficiency due to STK4 deficiency
	Synonym(s): (no synonyms)		Synonym(s): - CID due to STK4 deficiency

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

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

	External references: 5 OMIM references - 1 MeSH reference: D054091		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.