WormBase Tree Display for DO_term: DOID:0070094
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| DOID:0070094 | Name | oculocutaneous albinism type IA | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | An oculocutaneous albinism that has_material_basis_in an autosomal recessive null mutation of TYR on chromosome 11q14.3 with no residual protein activity. | ||||
| Synonym | Exact | OCA1A | |||
| Oculocutaneous Albinism, Tyrosinase-Negative | |||||
| Parent | Is_a | DOID:0050632 | |||
| DB_info | Database | OMIM | disease | 203100 | |
| Attribute_of | Gene_by_orthology | WBGene00009001 | |||
| WBGene00010661 | |||||
| WBGene00015332 | |||||
| WBGene00016419 | |||||
| WBGene00021553 |
