Leber Hereditary Optic Neuropathy, Autosomal Recessive 1 (LHONAR1)

Alias:

Leber Hereditary Optic Neuropathy, Autosomal Recessive

Mitochondrial Complex I Deficiency, Nuclear Type 38

Mc1dn38

Lhonar

Leber Hereditary Optic Neuropathy, Autosomal Recessive Autosomal Recessive

Lhonar1

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Leber Hereditary Optic Neuropathy, Autosomal Recessive 1, also known as leber hereditary optic neuropathy, autosomal recessive, is related to leber hereditary optic neuropathy, autosomal recessive 2 and leber hereditary optic neuropathy, modifier of. An important gene associated with Leber Hereditary Optic Neuropathy, Autosomal Recessive 1 is DNAJC30 (DnaJ Heat Shock Protein Family (Hsp40) Member C30). Related phenotypes are central scotoma and reduced visual acuity

Related ID：

MALACARDS：LBR040

OMIM：619382

MESH：D029242