Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8724
Gene Symbol: SNX3
SNX3
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
0.300 Biomarker GENOMICS_ENGLAND Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype. 12471201

2002