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#620029 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, LANGUAGE DELAY, AND SKELETAL DEFECTS WITH OR WITHOUT SEIZURES; NEDHLSS
Cytogenetic locations: 34163037
Gene summaries Genetic tests Medical literature
#618447 - LONG QT SYNDROME 8; LQT8
Cytogenetic locations: 25633834
#611875 - BRUGADA SYNDROME 3; BRGDA3
Cytogenetic locations: 17224476
#601005 - TIMOTHY SYNDROME; TS
Cytogenetic locations: 11q23.3
*114205 - CALCIUM CHANNEL, VOLTAGE-DEPENDENT, L TYPE, ALPHA-1C SUBUNIT; CACNA1C
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