|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_12117)|
|Downloads & Tools|
1 genes associated with the pulmonary alveolar microlithiasis phenotype from the curated OMIM Gene-Disease Associations dataset.
|SLC34A2||solute carrier family 34 (type II sodium/phosphate cotransporter), member 2|