Related MeSH Hierarchy (6)
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Abnormalities, Multiple » Ectodermal Dysplasia » Pachyonychia Congenita
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Skin Abnormalities » Ectodermal Dysplasia » Pachyonychia Congenita
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Skin Diseases, Genetic » Ectodermal Dysplasia » Pachyonychia Congenita
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Nail Diseases » Pachyonychia Congenita
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Abnormalities » Ectodermal Dysplasia » Pachyonychia Congenita
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Ectodermal Dysplasia » Pachyonychia Congenita
Description
A group of inherited ectodermal dysplasias whose most prominent clinical feature is hypertrophic nail dystrophy resulting in PACHYONYCHIA. Several specific subtypes of pachyonychia congenita have been associated with mutations in genes that encode KERATINS. MeSH
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Subtype Terms (1)
Phase 3 Indicated Drugs (1)
Phase 1 Indicated Drugs (6)
Other Experimental Indicated Drugs (1)
Organization Involved with Phase 3 Indications (3)
Organization Involved with Phase 2 Indications (1)
Organization Involved with Phase 1 Indications (3)
Organization Involved with Other Experimental Indications (1)
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