Disease #02206

Official abbreviation OLMSX
Name keratoderma, palmoplantar, mutilating, with periorificial keratotic plaques, X-linked (Olmsted syndrome, X-liked (OLMSX))
OMIM ID 300918
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MBTPS2
Associated tissues -
Disease features -
Remarks -

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