microphthalmia with limb anomalies Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/206920
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Genes

1 genes associated with the microphthalmia with limb anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SMOC1 SPARC related modular calcium binding 1