Showing entry for Amelogenesis Imperfecta, Type IB
| General Disease Information | |
|---|---|
| BXGD Id | BXGD008239 |
| Disease Name | Amelogenesis Imperfecta, Type IB |
| Disease CUI Id | C0399368 |
| MeSH Codes | C16 C07 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic 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
|