linear verrucous nevus syndrome
MONDO:0016831Mondo
Findings
No curated finding names linear verrucous nevus syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
27 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- AstrocytomaHPOHP:0009592
- Very frequent (80% to 99% of cases)
- HyperkeratosisHPOHP:0000962
- Very frequent (80% to 99% of cases)
- MacrocephalyHPOHP:0000256
- Very frequent (80% to 99% of cases)
- Neoplasm of the central nervous systemHPOHP:0100006
- Very frequent (80% to 99% of cases)
- Sparse scalp hairHPOHP:0002209
- Very frequent (80% to 99% of cases)
- Verrucous papuleHPOHP:0012500
- Very frequent (80% to 99% of cases)
- Mental deteriorationHPOHP:0001268
- Frequent (30% to 79% of cases)
- SeizureHPOHP:0001250
- Frequent (30% to 79% of cases)
- Abnormal cornea morphologyHPOHP:0000481
- Occasional (5% to 29% of cases)
- Abnormal skull morphologyHPOHP:0000929
- Occasional (5% to 29% of cases)
- Abnormality of the kidneyHPOHP:0000077
- Occasional (5% to 29% of cases)
- Aplasia/Hypoplasia of the corpus callosumHPOHP:0007370
- Occasional (5% to 29% of cases)
Show the remaining 15
- Aplasia/Hypoplasia of the foveaHPOHP:0008060
- Occasional (5% to 29% of cases)
- CataractHPOHP:0000518
- Occasional (5% to 29% of cases)
- Dandy-Walker malformationHPOHP:0001305
- Occasional (5% to 29% of cases)
- Genu recurvatumHPOHP:0002816
- Occasional (5% to 29% of cases)
- HypophosphatemiaHPOHP:0002148
- Occasional (5% to 29% of cases)
- Iris colobomaHPOHP:0000612
- Occasional (5% to 29% of cases)
Where it sits
- A kind of
Other names
1 name
Resolves to: linear verrucous nevus syndrome
- Also called
- linear hamartoma syndrome