Showing entry for Young Simpson syndrome
| General Disease Information | |
|---|---|
| BXGD Id | BXGD016183 |
| Disease Name | Young Simpson syndrome |
| Disease CUI Id | C1863557 |
| MeSH Codes | C23 C16 C11 C05 C10 C19 F03 F01 C14 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases; Mental Disorders; Behavior and Behavior Mechanisms; Cardiovascular Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:225 |
| Disease Ontology Class Name | syndrome |
| Disorder Network | disorder-protein-compound-food associations |
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