Disease #06359 (PEOB5 (?Progressive external ophthalmoplegia with Mi DNA deletions, autosomal recessive 5), OMIM:618098)

Official abbreviation PEOB5
Name ?Progressive external ophthalmoplegia with Mi DNA deletions, autosomal recessive 5
OMIM ID 618098
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene TOP3A
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

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00472231 - Verebi et al. (submitted) - F - France - - - - - PEOB5 Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy, Ptosis, Bilateral sensorineural hearing impairment, easy fatigability, progressive external ophtalmoplegia, exercice intolerance, hearing impairment, bilteral ptosis, weakness of facial musculature - TOP3A 2 1 Camille Verebi
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