Details of Disease

General Information of Disease (ID: DIS4XHR1)

Disease Name Combined oxidative phosphorylation deficiency 35
Synonyms COXPD35; combined oxidative phosphorylation deficiency 35
Disease Hierarchy
DISG5MW9: Combined oxidative phosphorylation deficiency
DIS4XHR1: Combined oxidative phosphorylation deficiency 35
Disease Identifiers
MONDO ID
MONDO_0054742
UMLS CUI
C4693466
OMIM ID
617873
MedGen ID
1639653

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
TRIT1 OTCU9FS5 Strong Autosomal recessive [1]
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References

1 Ultrasonic and postnatal findings in left visceral isomerism. Clin Exp Obstet Gynecol. 1991;18(2):75-9.