WormBase Tree Display for DO_term: DOID:14791
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| DOID:14791 | Name | Leber congenital amaurosis | |
|---|---|---|---|
| Status | Valid | ||
| Definition | A retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness. | ||
| Comment | Xref MGI. | ||
| Synonym | Exact | LCA | |
| Leber's amaurosis | |||
| Leber's congenital amaurosis | |||
| Leber's disease | |||
| Parent | Is_a | DOID:5679 | |
| DOID:0080015 | |||
| Child | Is (18) | ||
| Attribute_of | Gene_by_orthology | WBGene00000792 | |
| WBGene00002039 | |||
| WBGene00016966 |
