Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Nasu-Hakola disease (NHD), also referred to as polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL), is a rare inherited leukodystrophy characterized by progressive presenile dementia associated with recurrent bone fractures due to polycystic osseous lesions of the lower and upper extremities. (Orphanet Rare Disease Ontology, Orphanet_2770)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C536329
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Genes

2 genes/proteins associated with the disease Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
TREM2 triggering receptor expressed on myeloid cells 2 2.88009
TYROBP TYRO protein tyrosine kinase binding protein 2.88009