Ohtahara syndrome
neonatoal period electroclinical syndrome that is characterized by tonic spasms and partial seizures
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Ohtahara syndrome
Summary
Ohtahara syndrome is a designated intractable/rare disease[1]. It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Ohtahara syndrome's instance of is recorded as designated intractable/rare disease[3].
- Ohtahara syndrome's instance of is recorded as rare disease[4].
- Ohtahara syndrome's instance of is recorded as class of disease[5].
- Ohtahara syndrome is a type of neonatal period electroclinical syndrome[6].
- Ohtahara syndrome is a type of childhood onset epileptic encephalopathy[7].
- Ohtahara syndrome is a type of infantile epileptic encephalopathy[8].
- Ohtahara syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4381[9].
- Ohtahara syndrome's NCI Thesaurus ID is recorded as C116552[10].
- Ohtahara syndrome's NCI Thesaurus ID is recorded as C188139[11].
- Ohtahara syndrome's health specialty is recorded as neurology[12].
- Ohtahara syndrome's genetic association is recorded as SCN8A[13].
- Ohtahara syndrome's genetic association is recorded as ARX[14].
- Ohtahara syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050709[15].
- Ohtahara syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050709[16].
- Ohtahara syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
Ohtahara syndrome has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[2] It is known by 6 alternative names across languages and contexts.[18]