Showing entry for Carboxypeptidase N Deficiency
| General Disease Information | |
|---|---|
| BXGD Id | BXGD008231 |
| Disease Name | Carboxypeptidase N Deficiency |
| Disease CUI Id | C0398782 |
| MeSH Codes | C16 C18 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | |
| Disease Ontology Class Name | |
| Disorder Network | disorder-protein-compound-food associations
|