ODCs

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2 associated genes
No signs/symptoms info

COMMON GENES: 2

2 associated genes
No signs/symptoms info

Silver-Russell syndrome due to 11p15 microduplication

Silver-Russell syndrome due to imprinting defect of 11p15

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

Citations in the biomedical literature:

Silver-Russell syndrome due to 11p15 microduplication		Silver-Russell syndrome due to imprinting defect of 11p15

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: sporadic

	External references: No OMIM references No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.