Details of Disease | DrugMAP

General Information of Disease (ID: DISY3I1V)

Disease Name	Multiple mitochondrial dysfunctions syndrome 7
Disease Hierarchy	DISYBW5F: Fatal multiple mitochondrial dysfunctions syndrome DISY3I1V: Multiple mitochondrial dysfunctions syndrome 7
Disease Identifiers	MONDO ID MONDO_0957382 UMLS CUI C5830586 OMIM ID 620423 MedGen ID 1841222

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
GCSH	OTNC1OKA	Strong	Autosomal recessive	[1]
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References

1	Heterozygous GLDC and GCSH gene mutations in transient neonatal hyperglycinemia. Ann Neurol. 2002 Nov;52(5):643-6. doi: 10.1002/ana.10367.