|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Microphthalmia with limb anomalies, also known as ophthalmo-acromelic syndrome (OAS), is a rare developmental disorder characterized by bilateral microphthalmia or anophthalmia, synostosis, syndactyly, oligodactyly and/or polydactyly. (Orphanet Rare Disease Ontology, Orphanet_1106)|
|Downloads & Tools|
1 genes associated with the microphthalmia with limb anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
|SMOC1||SPARC related modular calcium binding 1|