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Disease table of CHROMOSOME 2P16.3 DELETION SYNDROME
OMIM ID: 614332
Gene-disease associations table
Gene
Associated with CHROMOSOME 2P16.3 DELETION SYNDROME in
Link to HGNC
Cytogenetic band
Number of associated diseases
Associated diseases
NRXN1
OMIM
HGNC link
2p16.3
2
614332
,
614325
Download the disease annotation in CSV format