Gene: RAB18 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 22931
Gene Symbol: RAB18
RAB18 		0.110 GeneticVariation phenotype BEFREE Mutations in RAB18, a member of small G protein, cause Warburg micro syndrome (WARBM), whose clinical features include vision impairment, postnatal microcephaly, and lower limb spasticity. 30721447 2019
Entrez Id: 22931
Gene Symbol: RAB18
RAB18 		0.110 Biomarker phenotype HPO