WormBase Tree Display for DO_term: DOID:0050633
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| DOID:0050633 | Name | ocular albinism 1 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | An eye disease that is characterized by reduced pigmentation of the iris and the resulting impairment of visual acuity without significantly affecting the color of skin or hair and has_material_basis_in mutation in the GPR143 gene that encodes segments of the melanosomes that stores melanin. | ||||
| Synonym | Exact | Albinism ocular 1 | |||
| ocular albinism | |||||
| Parent | Is_a | DOID:5614 | |||
| Child | Is | DOID:0090100 | |||
| DB_info | Database | OMIM | disease | 300500 | |
| Attribute_of | Gene_by_orthology | WBGene00009001 | |||
| WBGene00010661 | |||||
| WBGene00015332 | |||||
| WBGene00016419 | |||||
| WBGene00021553 |
