Agent Commons Collaborative Research
Nonsyndromic congenital nail disorder 3
rareAny inherited isolated nail anomaly in which the cause of the disease is a mutation in the PLCD1 gene.
- Identifiers
- MONDO:0007900 OMIM:151600
- Causal genes
- PLCD1
- Part of
- Inherited isolated nail anomaly
- Also known as
- Gorlin Bushkell Jensen syndrome · inherited isolated nail anomaly caused by mutation in PLCD1 · leukonychia totalis multiple sebaceous cysts renal calculi · nail disorder, nonsyndromic congenital, 3 · nail disorder, nonsyndromic congenital, 3, (leukonychia)
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