Details of Disease | DrugMAP

General Information of Disease (ID: DIS0Q3YM)

Disease Name	Silver-Russell syndrome 1
Synonyms	SRS1
Disease Hierarchy	DISSVJ1D: Silver-Russell syndrome DIS0Q3YM: Silver-Russell syndrome 1
Disease Identifiers	MONDO ID MONDO_0020796 UMLS CUI C5393125 OMIM ID 180860 MedGen ID 1718472

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
IGF2	TTE8WGO	Definitive	Autosomal dominant inheritance with maternal imprinting HP:0012275	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
IGF2	OTJ4O6MW	Definitive	Autosomal dominant inheritance with maternal imprinting HP:0012275	[1]
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References

1	Paternally Inherited IGF2 Mutation and Growth Restriction. N Engl J Med. 2015 Jul 23;373(4):349-56. doi: 10.1056/NEJMoa1415227. Epub 2015 Jul 8.