Disease

primary coenzyme Q10 deficiency 5

Name: primary coenzyme Q10 deficiency 5
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0070242 primary coenzyme Q10 deficiency 5 A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the COQ9 gene on chromosome 16q21. coenzyme Q10 deficiency, primary, 5 COQ10D5 encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome

Definition

A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the COQ9 gene on chromosome 16q21.

Synonyms

coenzyme Q10 deficiency, primary, 5
COQ10D5

Cross References

MIM:614654
ORDO:319678

Parent Terms

coenzyme Q10 deficiency disease

Child Terms

None

Sources of Associations

RGD
MGI
ZFIN
FB
WB
SGD

Associated Genes

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Associated Alleles

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Associated Models

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