Nonsyndromic congenital nail disorder 3

MONDO:0007900

Any inherited isolated nail anomaly in which the cause of the disease is a mutation in the PLCD1 gene.

Also known as: PLCD1 inherited isolated nail anomaly, inherited isolated nail anomaly caused by mutation in PLCD1, nail disorder, nonsyndromic congenital, 3, (leukonychia), nail disorder, nonsyndromic congenital, type 3, nonsyndromic congenital nail disorder type 3, Gorlin Bushkell Jensen syndrome, NDNC3, leukonychia Striatus

0 clinical trials for this condition and its sub-types, 0 tagged with Nonsyndromic congenital nail disorder 3 itself.

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Including sub-types (0) Tagged with Nonsyndromic congenital nail disorder 3 (0)

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