Disease #01485 (PC1 (pachyonychia congenita, type 1), OMIM:167200)

Official abbreviation PC1
Name pachyonychia congenita, type 1
OMIM ID 167200
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene KRT16
Associated tissues -
Disease features -
Remarks -