Showing entry for HERMANSKY-PUDLAK SYNDROME 2
| General Disease Information | |
|---|---|
| BXGD Id | BXGD014510 |
| Disease Name | HERMANSKY-PUDLAK SYNDROME 2 |
| Disease CUI Id | C1842362 |
| MeSH Codes | C16 C18 C11 C17 C15 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:630 |
| Disease Ontology Class Name | genetic disease |
| Disorder Network | disorder-protein-compound-food associations
|