Disease #01318 (Cylindromatosis, familial, OMIM:132700)

Official abbreviation -
Name Cylindromatosis, familial
OMIM ID 132700
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 CYLD
Associated tissues -
Disease features -
Remarks -