ODCs

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5 OMIM references -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Autosomal dominant progressive external ophthalmoplegia

Glucocorticoid resistance


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SLC25A4	(0.62)	NR3C1

Citations in the biomedical literature:

Autosomal dominant progressive external ophthalmoplegia		Glucocorticoid resistance
	Synonym(s): - adPEO		Synonym(s): (no synonyms)

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare urogenital disease

	Classification (ICD10): - Diseases of the eye and adnexa -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: 5 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.