Meier-Gorlin syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An autosomal recessive disorder characterized by severe intrauterine and postnatal growth retardation, microcephaly, bilateral microtia and hypoplastic patellae. (Human Disease Ontology, DOID_0060306)
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5 genes/proteins associated with the disease Meier-Gorlin syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CDT1 chromatin licensing and DNA replication factor 1 2.88009
CDC6 cell division cycle 6 2.88009
ORC6 origin recognition complex, subunit 6 2.88009
ORC4 origin recognition complex, subunit 4 2.88009
ORC1 origin recognition complex, subunit 1 2.88009