Search Ontology:
Human Disease

visual impairment and progressive phthisis bulbi

Term ID
DOID:0070356
Synonyms
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. (3)
References
Ontology
Human Disease   ( DOID:0070356 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models
Citations