ODCs

Click node...

3 associated genes
No signs/symptoms info

COMMON GENES: 2

2 associated genes
No signs/symptoms info

Beckwith-Wiedemann syndrome due to imprinting defect of 11p15

Silver-Russell syndrome due to imprinting defect of 11p15

Citations in the biomedical literature:

Beckwith-Wiedemann syndrome due to imprinting defect of 11p15		Silver-Russell syndrome due to imprinting defect of 11p15

	Classification (Orphanet): - Rare cardiac disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare maxillo-facial surgical disease - Rare oncologic disease - Rare otorhinolaryngologic disease - Rare renal 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: neonatal/infancy Average age of death: - Type of inheritance: sporadic		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.