Leber hereditary optic neuropathy
Human disease
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Leber hereditary optic neuropathy
Summary
Leber hereditary optic neuropathy is a designated intractable/rare disease[1]. It has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Leber hereditary optic neuropathy's instance of is recorded as designated intractable/rare disease[3].
- Leber hereditary optic neuropathy's instance of is recorded as developmental defect during embryogenesis[4].
- Leber hereditary optic neuropathy's instance of is recorded as class of disease[5].
- Theodor Leber is named after Leber hereditary optic neuropathy[6].
- Leber hereditary optic neuropathy is a type of optic nerve disease[7].
- Leber hereditary optic neuropathy is a type of hereditary optic atrophy[8].
- Leber hereditary optic neuropathy is a type of genetic peripheral neuropathy[9].
- Leber hereditary optic neuropathy is a type of mitochondrial disease with eye involvement[10].
- Leber hereditary optic neuropathy is a type of hereditary optic neuropathy[11].
- Leber hereditary optic neuropathy is a type of mitochondrial disease with dilated cardiomyopathy[12].
- Leber hereditary optic neuropathy is a type of mitochondrial disease with hypertrophic cardiomyopathy[13].
- Leber hereditary optic neuropathy is a type of mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA[14].
- Leber hereditary optic neuropathy is a type of disease[15].
- Leber hereditary optic neuropathy's Commons category is recorded as Leber's hereditary optic neuropathy[16].
- Leber hereditary optic neuropathy's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4660[17].
- Leber hereditary optic neuropathy's NCI Thesaurus ID is recorded as C84808[18].
- Leber hereditary optic neuropathy's health specialty is recorded as ophthalmology[19].
- Leber hereditary optic neuropathy's genetic association is recorded as ATP6[20].
- Leber hereditary optic neuropathy's genetic association is recorded as ND4[21].
- Leber hereditary optic neuropathy's genetic association is recorded as ND2[22].
- Leber hereditary optic neuropathy's genetic association is recorded as ND4L[23].
- Leber hereditary optic neuropathy's genetic association is recorded as CYTB[24].
- Leber hereditary optic neuropathy's genetic association is recorded as ND6[25].
- Leber hereditary optic neuropathy's genetic association is recorded as ND5[26].
- Leber hereditary optic neuropathy's genetic association is recorded as ND1[27].
Why It Matters
Leber hereditary optic neuropathy has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[2] It is known by 14 alternative names across languages and contexts.[28]