Disease #00149

Official abbreviation LDYT
Name LEBER OPTIC ATROPHY AND DYSTONIA, alt: LEBER HEREDITARY OPTIC NEUROPATHY WITH DYSTONIA; LDYT;; DYSTONIA, FAMILIAL, WITH VISUAL FAILURE AND STRIATAL LUCENCIES;; MARSDEN SYNDROME
OMIM ID 500001
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 4 genes MT-ND1, MT-ND3, MT-ND4, MT-ND6
Associated tissues -
Disease features -
Remarks -

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