Disease #00032

Official abbreviation PLOSL
Name polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL)
OMIM ID 221770
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 2 genes TREM2, TYROBP
Associated tissues -
Disease features -
Remarks -