Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55704
Gene Symbol: CCDC88A
CCDC88A
CUI: C0025958
Disease: Microcephaly
Microcephaly 		0.300 Biomarker GENOMICS_ENGLAND A novel homozygous nonsense mutation in CCDC88A gene cause PEHO-like syndrome in consanguineous Saudi family. 30392057

2019