juvenile neuronal ceroid lipofuscinosis
extremely rare and fatal autosomal recessive neurodegenerative disorder in humans
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juvenile neuronal ceroid lipofuscinosis
Summary
juvenile neuronal ceroid lipofuscinosis is a rare disease[1]. It draws 697 Wikipedia views per month (rare_disease category, ranking #88 of 627).[2]
Key Facts
- juvenile neuronal ceroid lipofuscinosis's instance of is recorded as rare disease[3].
- juvenile neuronal ceroid lipofuscinosis's instance of is recorded as class of disease[4].
- Frederick Batten is named after juvenile neuronal ceroid lipofuscinosis[5].
- juvenile neuronal ceroid lipofuscinosis is a type of neuronal ceroid lipofuscinosis[6].
- juvenile neuronal ceroid lipofuscinosis's Commons category is recorded as Batten disease[7].
- juvenile neuronal ceroid lipofuscinosis's ICPC 2 ID is recorded as T99[8].
- juvenile neuronal ceroid lipofuscinosis's health specialty is recorded as endocrinology[9].
- juvenile neuronal ceroid lipofuscinosis's genetic association is recorded as CTSD[10].
- juvenile neuronal ceroid lipofuscinosis's genetic association is recorded as CLN8[11].
- juvenile neuronal ceroid lipofuscinosis's genetic association is recorded as CLN3[12].
- juvenile neuronal ceroid lipofuscinosis's genetic association is recorded as PPT1[13].
- juvenile neuronal ceroid lipofuscinosis's genetic association is recorded as TPP1[14].
- juvenile neuronal ceroid lipofuscinosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79264[15].
- juvenile neuronal ceroid lipofuscinosis's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
juvenile neuronal ceroid lipofuscinosis draws 697 Wikipedia views per month (rare_disease category, ranking #88 of 627).[2] It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[17] It is known by 35 alternative names across languages and contexts.[18]