Showing entry for Pelger-Huet Anomaly
| General Disease Information | |
|---|---|
| BXGD Id | BXGD002252 |
| Disease Name | Pelger-Huet Anomaly |
| Disease CUI Id | C0030779 |
| MeSH Codes | C16 C15 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | HP:0002715 HP:0001871 |
| Human Phenotype Ontology Term | Abnormality of the immune system; Abnormality of blood and blood-forming tissues |
| Disease Ontology Id | DOID:630 |
| Disease Ontology Class Name | genetic disease |
| Disorder Network | disorder-protein-compound-food associations
|