WormBase Tree Display for DO_term: DOID:0070094
expand all nodes | collapse all nodes | view schema
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 (5) |