Showing entry for Lissencephaly
| General Disease Information | |
|---|---|
| BXGD Id | BXGD005675 |
| Disease Name | Lissencephaly |
| Disease CUI Id | C0266463 |
| MeSH Codes | C16 C10 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| Semantic Type | Congenital Abnormality |
| Human Phenotype Ontology Id | HP:0000707 |
| Human Phenotype Ontology Term | Abnormality of the nervous system |
| Disease Ontology Id | DOID:630 DOID:7 DOID:225 DOID:150 DOID:0080015 |
| Disease Ontology Class Name | genetic disease; disease of anatomical entity; syndrome; disease of mental health; physical disorder |
| Disorder Network | disorder-protein-compound-food associations
|