Showing entry for LAURIN-SANDROW SYNDROME
| General Disease Information | |
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| BXGD Id | BXGD015194 |
| Disease Name | LAURIN-SANDROW SYNDROME |
| Disease CUI Id | C1851100 |
| MeSH Codes | C16 C05 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | HP:0040064 HP:0000924 |
| Human Phenotype Ontology Term | Abnormality of limbs; Abnormality of the skeletal system |
| Disease Ontology Id | DOID:7 |
| Disease Ontology Class Name | disease of anatomical entity |
| Disorder Network | disorder-protein-compound-food associations |
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