Showing entry for HOYERAAL-HREIDARSSON SYNDROME
| General Disease Information | |
|---|---|
| BXGD Id | BXGD014785 |
| Disease Name | HOYERAAL-HREIDARSSON SYNDROME |
| Disease CUI Id | C1846142 |
| MeSH Codes | C23 C16 C13 C17 C05 C10 F03 C15 F01 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Hemic and Lymphatic Diseases; Behavior and Behavior Mechanisms |
| 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
|