Meier-Gorlin syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An autosomal recessive disorder characterized by severe intrauterine and postnatal growth retardation, microcephaly, bilateral microtia and hypoplastic patellae. (Human Disease Ontology, DOID_0060306)
External Link http://www.omim.org/entry/224690
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Genes

1 genes associated with the Meier-Gorlin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
ORC1 origin recognition complex, subunit 1