Showing entry for Chromosome 2q32-Q33 Deletion Syndrome
| General Disease Information | |
|---|---|
| BXGD Id | BXGD017342 |
| Disease Name | Chromosome 2q32-Q33 Deletion Syndrome |
| Disease CUI Id | C2676739 |
| MeSH Codes | C23 C16 C10 F03 F01 |
| Disease Class Name | Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| Semantic Type | Disease or Syndrome |
| 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
|