Disease #00032 (PLOSL1 (polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL)), OMIM:221770)

Official abbreviation PLOSL1
Name polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL)
OMIM ID 221770
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 2 genes TREM2, TYROBP
Associated tissues -
Disease features -
Remarks -
Date created 2012-08-28 13:31:38 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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