About   Help   FAQ
Disease Ontology Browser
oculocutaneous albinism type IB (DOID:0070095)
Alliance: disease page
Synonyms: Albinism, Yellow Mutant Type; OCA1B
Alt IDs: OMIM:606952, MESH:C537729
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory