neurofibromatoses
human diseases
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Summary
neurofibromatoses is a designated intractable/rare disease[1]. neurofibromatoses draws 9,166 Wikipedia views per month (designated intractable rare disease category, ranking #31 of 201).[2]
Key Facts
- Instance of: rare disease[3], class of disease[4], symptom or sign[5]
- Subclass of: autosomal dominant disease[6], peripheral nervous system neoplasm[7], overgrowth syndrome[8], disease[9]
- Commons category: Neurofibromatosis[10]
- ICPC 2 ID: A90[11]
- External data available at URL: http://www.nanbyou.or.jp/entry/5361[12]
- ICD-9-CM: 237.70[13], 237.72[14], 237.7[15], 237.71[16]
- NCI Thesaurus ID: C6727[17], C3274[18], C3273[19]
- Health specialty: medical genetics[20], neurology[21]
- Genetic association: NF1[22], NF2[23]
- Exact match: http://purl.obolibrary.org/obo/DOID_8712[24], http://identifiers.org/doid/DOID:8712[25], http://purl.obolibrary.org/obo/HP_0001067[26], http://www.orpha.net/ORDO/Orphanet_636[27], http://www.orpha.net/ORDO/Orphanet_637[28], http://www.orpha.net/ORDO/Orphanet_93921[29]
Why It Matters
neurofibromatoses has Wikipedia articles in 25 language editions, a strong signal of global cultural recognition.[30] neurofibromatoses is known by 61 alternative names across languages and contexts.[31]