WormBase Tree Display for DO_term: DOID:0070095
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DOID:0070095 | Name | oculocutaneous albinism type IB | |||
---|---|---|---|---|---|
Status | Valid | ||||
Definition | An oculocutaneous albinism that has_material_basis_in an autosomal recessive hypomorphic mutation of TYR on chromosome 11q14.3 with retention of some residual protein activity. | ||||
Synonym | Exact | Albinism, Yellow Mutant Type | |||
OCA1B | |||||
Parent | Is_a | DOID:0050632 | |||
DOID:0080578 | |||||
DB_info | Database | OMIM | disease | 606952 | |
Attribute_of | Gene_by_orthology | WBGene00009001 | |||
WBGene00010661 | |||||
WBGene00015332 | |||||
WBGene00016419 | |||||
WBGene00021553 |