Details of Disease | DrugMAP

General Information of Disease (ID: DIS37TLQ)

Disease Name	Arthrogryposis multiplex congenita 5
Synonyms	ARTHROGRYPOSIS MULTIPLEX CONGENITA 5; AMC5
Disease Hierarchy	DISMCQP6: Arthrogryposis multiplex congenita DIS37TLQ: Arthrogryposis multiplex congenita 5
Disease Identifiers	MONDO ID MONDO_0100218 UMLS CUI C5436453 OMIM ID 618947 MedGen ID 1731112

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
TOR1A	TTF85KW	Strong	Autosomal recessive	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
TOR1A	OTYCLGJU	Strong	Autosomal recessive	[1]
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References

1	Dystonia and the nuclear envelope. Neuron. 2005 Dec 22;48(6):875-7. doi: 10.1016/j.neuron.2005.12.006.