Gene: HCCS ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3052
Gene Symbol: HCCS
HCCS 		0.010 GeneticVariation disease BEFREE FDH shows some clinical overlap with the microphthalmia with linear skin defects (MLS) syndrome, another X-linked male lethal condition, associated with mutations of HCCS in the majority of cases. 19277062 2009