multiple familial trichoepithelioma
human disease
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Summary
multiple familial trichoepithelioma is a rare disease[1]. It ranks in the top 3% of rare disease entities by monthly Wikipedia readership (74 views/month).[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: Brooke-Spiegler syndrome[4], trichoepithelioma[5], head and neck disease[6], hereditary disorder[7]
- Genetic association: CYLD[8]
- Age of onset: childhood onset[9]
- Exact match: http://www.orpha.net/ORDO/Orphanet_79493[10], http://www.orpha.net/ORDO/Orphanet_867[11]
- Has phenotype: papule[12], Q141816715[13], basal-cell carcinoma of the skin[14]
- P14914: D00867[15]
Why It Matters
multiple familial trichoepithelioma is known by 10 alternative names across languages and contexts.[16]