Search Ontology:

Human Disease

chronic progressive external ophthalmoplegia

Term ID

DOID:12558

Synonyms

progressive external ophthalmoplegia

Definition

References

GARD:4503
ICD10CM:H49.4
ICD9CM:378.72
MESH:D017246
MIM:PS157640
SNOMEDCT_US_2023_03_01:194126004
UMLS_CUI:C0162674

Ontology

Human Disease ( DOID:12558 )

Relationships

is a type of: mitochondrial myopathy

mitochondrial myopathy Show first 5 Terms
has subtype: autosomal dominant progressive external ophthalmoplegia 1 autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5 ... Show All 12 Terms

autosomal dominant progressive external ophthalmoplegia 1 autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5 autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6 autosomal recessive progressive external ophthalmoplegia 1 autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2 autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3 autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4 autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5 Kearns-Sayre syndrome Show first 5 Terms

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Alliance (1)

Genes Involved

Zebrafish Models