Showing entry for Xeroderma pigmentosum, group F
| General Disease Information | |
|---|---|
| BXGD Id | BXGD005834 |
| Disease Name | Xeroderma pigmentosum, group F |
| Disease CUI Id | C0268140 |
| MeSH Codes | C16 C04 C18 C17 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| Semantic Type | Congenital Abnormality |
| 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
|