Agent Commons Collaborative Research
Nevoid basal cell carcinoma syndrome
rareA rare hereditary disorder due to autosomal dominant transmission with hamartosis characterized by multiple early-onset basal cell carcinoma (BCC), multiple jaw keratocysts and skeletal abnormalities.
- Identifiers
- MONDO:0007187 Orphanet:377
- Part of
- Autosomal dominant diseaseDevelopmental defect during embryogenesisHereditary neoplastic syndromeHereditary neurological diseaseNeurocutaneous syndrome
- Also known as
- basal cell nevus syndrome · BCNS · Gorlin syndrome · Gorlin-Goltz syndrome · multiple basal cell carcinomas
Subtypes
| Disease | Subtypes |
|---|---|
| Basal cell nevus syndrome 1 | |
| Basal cell nevus syndrome 2 |
Rare disease
Projects
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