{{Rsnum
|rsid=386833840
|Chromosome=19
|Orientation=minus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=TYROBP
|position=35907534
|Gene_s=TYROBP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=19
|CLNACC=RCV000049808.1
|CLNALLE=1
|CLNDBN=Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1197:C1857316:221770:2770
|CLNHGVS=NC_000019.9:g.36398436delC
|CLNSIG=4
|Disease=Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
|FwdREF=G
|REF=TC
|RSPOS=36398435
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386833840
|GENEINFO=TYROBP:7305
|GENE_ID=7305
|GENE_NAME=TYROBP
}}{{PMID Auto
|PMID=10888890
|Title=Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts.
}}

{{PMID Auto
|PMID=12370476
|Title=Heterogeneity of presenile dementia with bone cysts (Nasu-Hakola disease): three genetic forms.
}}

{{PMID Auto
|PMID=15883308
|Title=The genetic causes of basal ganglia calcification, dementia, and bone cysts: DAP12 and TREM2.
}}

{{PMID Auto
|PMID=17125796
|Title=A novel compound heterozygous mutation in the DAP12 gene in a patient with Nasu-Hakola disease.
}}

{{PMID Auto
|PMID=22082900
|Title=A Japanese case with Nasu-Hakola disease of DAP12 gene mutation exhibiting precuneus hypoperfusion.
}}