| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Lenz-Majewski hyperostotic dwarfism is an extremely rare syndrome associating dwarfism, characteristic facial appearance, cutis laxa and progressive bone sclerosis. (Orphanet Rare Disease Ontology, Orphanet_2658) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C537115 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Lenz Majewski hyperostotic dwarfism from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| PTDSS1 | phosphatidylserine synthase 1 | 2.88009 |
