OMIM Links for GEO Profiles (Select 86578150) - OMIM - NCBI

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Links from GEO Profiles

Items: 5

Select item 6200291.

#620029 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, LANGUAGE DELAY, AND SKELETAL DEFECTS WITH OR WITHOUT SEIZURES; NEDHLSS

Cytogenetic locations: -

OMIM:: 620029

Gene summaries Genetic tests Medical literature

Select item 6184472.

#618447 - LONG QT SYNDROME 8; LQT8

Cytogenetic locations: -

OMIM:: 618447

Gene summaries Genetic tests Medical literature

Select item 6118753.

#611875 - BRUGADA SYNDROME 3; BRGDA3

Cytogenetic locations: -

OMIM:: 611875

Gene summaries Genetic tests Medical literature

Select item 6010054.

#601005 - TIMOTHY SYNDROME; TS

Cytogenetic locations: -

OMIM:: 601005

Gene summaries Genetic tests Medical literature

Select item 1142055.

*114205 - CALCIUM CHANNEL, VOLTAGE-DEPENDENT, L TYPE, ALPHA-1C SUBUNIT; CACNA1C

Cytogenetic locations: 30172029

OMIM:: 114205

Gene summaries Genetic tests Medical literature

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OMIM Links for GEO Profiles (Select 86578150) (5)
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