ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Silver-Russell syndrome due to 11p15 microduplication

Familial retinal arterial macroaneurysm

H19	(OMIM)		IGFBP7	(UniProt - OMIM)
IGF2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	IGF2	(0.75)	IGFBP7

Citations in the biomedical literature:

Silver-Russell syndrome due to 11p15 microduplication		Familial retinal arterial macroaneurysm
	Synonym(s): (no synonyms)		Synonym(s): - FRAM - Retinal arterial macroaneurysm and supravalvular pulmonic stenosis

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare surgical cardiac disease

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

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

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

No signs/symptoms info available.