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Autosomal dominant progressive external ophthalmoplegia
5 OMIM references -
5 associated genes
48 connected diseases
No signs/symptoms info
Disease Type of connection
Mitochondrial neurogastrointestinal encephalomyopathy
Sensory ataxic neuropathy - dysarthria - ophthalmoparesis
Alpers syndrome
Autosomal recessive progressive external ophthalmoplegia
Recessive mitochondrial ataxia syndrome
Spinocerebellar ataxia with epilepsy
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
Congenital cataract - hypertrophic cardiomyopathy - mitochondrial myopathy
Infantile onset spinocerebellar ataxia
Kearns-Sayre syndrome
Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
Mitochondrial DNA depletion syndrome, hepatocerebrorenal form
Giant cell glioblastoma
Gliosarcoma
B-cell chronic lymphocytic leukemia
Precursor B-cell acute lymphoblastic leukemia
Adrenocortical carcinoma
Essential thrombocythemia
Familial pancreatic carcinoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Young adult-onset Parkinsonism
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Complete androgen insensitivity syndrome
Familial hypospadias
Kennedy disease
Partial androgen insensitivity syndrome
Hypohidrotic ectodermal dysplasia with immunodeficiency
Amyotrophic lateral sclerosis
Ataxia-telangiectasia
Ataxia-telangiectasia variant
Combined cervical dystonia
Mantle cell lymphoma
Autosomal agammaglobulinemia
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Burkitt lymphoma
CLN3 disease
CLN5 disease
Craniometaphyseal dysplasia
Heritable pulmonary arterial hypertension
Hyper-IgM syndrome type 2
Hypoplastic left heart syndrome
Oculodentodigital dysplasia
Precursor T-cell acute lymphoblastic leukemia
Syndactyly type 3
Glucocorticoid resistance
Familial isolated congenital asplenia
Synonym(s):
- adPEO
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (ICD10):
- Diseases of the eye and adnexa -
Epidemiological data:
(no data available)
External references:
5 OMIM references -
No MeSH references
No signs/symptoms info available.