Oguchi disease-1
human disease
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Oguchi disease-1
Summary
Oguchi disease-1 is a rare disease[1]. It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Oguchi disease-1's instance of is recorded as rare disease[3].
- Oguchi disease-1's instance of is recorded as class of disease[4].
- Oguchi disease-1 is a type of congenital stationary night blindness[5].
- Oguchi disease-1 is a type of genetic disease[6].
- Oguchi disease-1 is a type of autosomal recessive disease[7].
- Oguchi disease-1's symptoms and signs is recorded as Mizuo–Nakamura phenomenon[8].
- Oguchi disease-1's health specialty is recorded as neurology[9].
- Oguchi disease-1's genetic association is recorded as SAG[10].
- Oguchi disease-1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110712[11].
- Oguchi disease-1's exact match is recorded as http://identifiers.org/doid/DOID:0110712[12].
- Oguchi disease-1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_75382[13].
- Oguchi disease-1's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
Oguchi disease-1 has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] It is known by 6 alternative names across languages and contexts.[15]