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Diseases

Isolated Complex I Deficiency

isolated complex i deficiency

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

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Core Information

Disease Name
Isolated Complex I Deficiency
Standard Disease Name
isolated complex i deficiency
MeSH Tree
No data
ICD-10
G71.3

Identifiers

DO ID
No data
MeSH ID
C537475
OMIM ID
252010
UMLS ID
C2936907
HPO ID
No data

Description and Extensions

Description
Isolated complex I deficiency is a rare inborn error of metabolism due to mutations in nuclear or mitochondrial genes encoding subunits or assembly factors of the human mitochondrial complex I (NADH:
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