|Name||microphthalmia or anophthalmia and associated anomalies|
|NCBI Gene ID||4080|
|Expression in Tissues and Cell Lines||
MAA has 1 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 1 datasets.
Click the + buttons to view associations for MAA from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with MAA gene/protein from the curated CTD Gene-Disease Associations dataset.|