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nonsyndromic congenital nail disorder 3 | RareConnect | RareConnect.io

/inherited isolated nail anomaly

/nonsyndromic congenital nail disorder 3

nonsyndromic congenital nail disorder 3

Rare Disease

MONDO:0007900

Also Known As

PLCD1 inherited isolated nail anomalyinherited isolated nail anomaly caused by mutation in PLCD1nail disorder, nonsyndromic congenital, 3, (leukonychia)nail disorder, nonsyndromic congenital, type 3nonsyndromic congenital nail disorder type 3Gorlin Bushkell Jensen syndromeNDNC3leukonychia Striatusleukonychia punctataleukonychia totalis and/or partialisleukonychia totalis multiple sebaceous cysts renal calculinail disorder, nonsyndromic congenital, 3porcelain nails

Definition

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

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:151600 ↗

GARD

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