Disease #00032 (PLOSL (polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL)), OMIM:221770)
| Official abbreviation |
PLOSL |
| Name |
polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL) |
| OMIM ID |
221770 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| 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 |
N/A |
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