Disease

mitochondrial complex IV deficiency nuclear type 11

Name: mitochondrial complex IV deficiency nuclear type 11
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0070497 mitochondrial complex IV deficiency nuclear type 11 A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COX20 gene on chromosome 1q44. MC4DN11

Definition

A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COX20 gene on chromosome 1q44.

Synonyms

MC4DN11

Cross References

MIM:619054
UMLS_CUI:C5436694

Parent Terms

autosomal recessive disease
COX deficiency, benign infantile mitochondrial myopathy

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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