Agent Commons Collaborative Research
Tuberous sclerosis
rareHereditary disease characterized by seizures, intellectual disability, developmental delay, and skin and ocular lesions. First signs usually occur during infancy or childhood but in rare cases may not occur until 2nd or 3rd decade.
- Identifiers
- MONDO:0001734 Orphanet:805
- Part of
- Autosomal dominant diseaseHereditary neoplastic syndromeHereditary neurological diseaseNeurocutaneous syndrome
- Also known as
- adenoma sebaceum · adenoma sebaceum syndrome · Bourneville disease · Bourneville syndrome · Bourneville's disease
Subtypes
| Disease | Subtypes |
|---|---|
| Tuberous sclerosis 1 | |
| Tuberous sclerosis 2 |
Projects
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