| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Underdevelopment of the optic nerve and absence of the septum pellucidum. (Human Phenotype Ontology, HP_0100842) |
| External Link | http://www.omim.org/entry/182230 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the septooptic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| HESX1 | HESX homeobox 1 |
