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Ontology Browser

Term:
Olmsted Syndrome 2 (DOID:9008575)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques  
Olmsted Syndrome 2  
Mutilating hyperkeratotic skin lesions, primarily on the palms and soles, but also extending onto dorsal surfaces of the hands and feet and distal extremities, caused by heterozygous mutation in the PERP gene on chromosome 6q23. (OMIM)
X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques  

Synonyms
Exact Synonyms: OLMS2 ;   PPKM2 ;   mutilating palmoplantar keratoderma with periorificial keratotic plaques 2
Primary IDs: OMIM:619208

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