Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 3 (PEOB3)

Alias:

Peob3

Progressive External Ophthalmoplegia, Autosomal Recessive 3

Autosomal Recessive Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions 3

Progressive External Ophthalmoplegia with Mi Dna Deletions, Autosomal Recessive 3

Autosomal Recessive Progressive External Ophthalmoplegia 3

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 3, is also known as peob3. An important gene associated with Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 3 is TK2 (Thymidine Kinase 2). Affiliated tissues include skeletal muscle, and related phenotypes are ptosis and dysphagia

Related ID：

MALACARDS：PRG129

OMIM：617069

MESH：D017246