Nasu-Hakola disease
human disease
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Nasu-Hakola disease
Summary
Nasu-Hakola disease is a developmental defect during embryogenesis[1]. It draws 9 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #127 of 308).[2]
Key Facts
- Nasu-Hakola disease's instance of is recorded as developmental defect during embryogenesis[3].
- Nasu-Hakola disease's instance of is recorded as designated intractable/rare disease[4].
- Nasu-Hakola disease's instance of is recorded as rare disease[5].
- Nasu-Hakola disease's instance of is recorded as class of disease[6].
- Nasu-Hakola disease is a type of autosomal recessive disease[7].
- Nasu-Hakola disease is a type of nervous system heredodegenerative disease[8].
- Nasu-Hakola disease is a type of primary osteolysis[9].
- Nasu-Hakola disease's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4256[10].
- Nasu-Hakola disease's ICD-9-CM is recorded as 758.89[11].
- Nasu-Hakola disease's genetic association is recorded as TYROBP[12].
- Nasu-Hakola disease's genetic association is recorded as TREM2[13].
- Nasu-Hakola disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090112[14].
- Nasu-Hakola disease's exact match is recorded as http://identifiers.org/doid/DOID:0090112[15].
- Nasu-Hakola disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2770[16].
- Nasu-Hakola disease's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
Nasu-Hakola disease draws 9 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #127 of 308).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[18] It is known by 16 alternative names across languages and contexts.[19]