Brooke-Spiegler syndrome
Human disease
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Summary
Brooke-Spiegler syndrome is a rare disease[1]. It is known by 3 alternative names across languages and contexts.[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: autosomal dominant disease[4], skin disease[5]
- Prevalence: 0.000001[6]
- Genetic association: CYLD[7]
- Age of onset: juvenile onset[8], adult onset[9]
- Exact match: http://purl.obolibrary.org/obo/DOID_0050693[10], http://identifiers.org/doid/DOID:0050693[11]
- On focus list of Wikimedia project: WikiProject Medicine[12]
- Has phenotype: Q141816406[13], epidermal appendage tumor[14], Q141816290[15], nodule[16], Q141815113[17], basal-cell carcinoma of the skin[18], Q141815980[19], Q141816309[20], ulcer[21], deafness[22], visual impairment[23], Q141815955[24], Q141815956[25], Bell's palsy[26]
- P14914: D79493[27]