visual impairment and progressive phthisis bulbi Disease Ontology Browser

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Disease Ontology Browser

visual impairment and progressive phthisis bulbi (DOID:0070356)
Alliance: disease page
Alt IDs: OMIM:618283, MESH:D005128
Definition: An eye disease that is characterized by poor vision at birth, with development of bilateral phthisis by adulthood and that has_material_basis_in homozygous mutation in the MARK3 gene on chromosome 14q3.

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)
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