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Disease table of RETT SYNDROME
OMIM ID: 312750
Gene-disease associations table
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Gene
Associated with RETT SYNDROME in
Link to HGNC
Cytogenetic band
Number of associated diseases
Associated diseases
MECP2
ClinVar, OMIM, HUMSAVAR
HGNC link
Xq28
6
300673
,
PS309510
,
PS209850
,
312750
,
143465
,
105830
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