ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Growth retardation-mild developmental delay-chronic hepatitis syndrome

Familial papillary renal cell carcinoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SH2B3	(0.72)	MET

Citations in the biomedical literature:

Growth retardation-mild developmental delay-chronic hepatitis syndrome		Familial papillary renal cell carcinoma

	Classification (Orphanet): - Rare genetic disease - Rare hepatic disease		Classification (Orphanet): - Rare genetic disease - Rare oncologic disease - Rare renal disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Neoplasms -

	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: - Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C538614

No signs/symptoms info available.