Showing entry for Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
| General Disease Information | |
|---|---|
| BXGD Id | BXGD018131 |
| Disease Name | Hyper-Immunoglobulin E Syndrome, Autosomal Dominant |
| Disease CUI Id | C2936739 |
| MeSH Codes | C16 C20 C15 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:630 DOID:7 |
| Disease Ontology Class Name | genetic disease; disease of anatomical entity |
| Disorder Network | disorder-protein-compound-food associations |
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