ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Growth retardation-mild developmental delay-chronic hepatitis syndrome

Periventricular nodular heterotopia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SH2B3	(0.77)	FLNA

Citations in the biomedical literature:

Growth retardation-mild developmental delay-chronic hepatitis syndrome		Periventricular nodular heterotopia

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

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

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

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

No signs/symptoms info available.