Details of Disease | DrugMAP

General Information of Disease (ID: DISRJPAS)

Disease Name	Autosomal dominant Robinow syndrome 3
Synonyms	autosomal dominant Robinow syndrome type 3; Robinow syndrome, autosomal dominant type 3; DVL3 Robinow syndrome; Robinow syndrome, autosomal dominant 3; Robinow syndrome caused by mutation in DVL3; DRS3
Definition	Any Robinow syndrome in which the cause of the disease is a mutation in the DVL3 gene.
Disease Hierarchy	DIS94N80: Autosomal dominant Robinow syndrome DISK1CNU: Robinow syndrome DISRJPAS: Autosomal dominant Robinow syndrome 3
Disease Identifiers	MONDO ID MONDO_0014819 UMLS CUI C4225164 OMIM ID 616894 MedGen ID 907878

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
DVL3	OTPRROHJ	Strong	Autosomal dominant	[1]
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References

1	Mercury in the dental profession: a neglected problem. J Conn State Dent Assoc. 1979 Summer;53(3):111-2.