Showing entry for Irido-corneo-trabecular dysgenesis (disorder)
| General Disease Information | |
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| BXGD Id | BXGD007695 |
| Disease Name | Irido-corneo-trabecular dysgenesis (disorder) |
| Disease CUI Id | C0344559 |
| MeSH Codes | C16 C11 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| Semantic Type | Congenital Abnormality |
| Human Phenotype Ontology Id | HP:0000478 |
| Human Phenotype Ontology Term | Abnormality of the eye |
| Disease Ontology Id | DOID:630 DOID:7 |
| Disease Ontology Class Name | genetic disease; disease of anatomical entity |
| Disorder Network | disorder-protein-compound-food associations |
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