Personal stories - OMIM - NCBI

Personal stories - OMIM - NCBI



From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.

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• Search OMIM for "Personal stories" 

#601144 - BRUGADA SYNDROME 1; BRGDA1

CARDIAC CONDUCTION DEFECT, NONSPECIFIC, INCLUDED

Cytogenetic locations: 3p22.2

OMIM:

 

601144

Gene summaries Genetic tests Medical literature

Select item 6103822.

%610382 - PROSOPAGNOSIA, HEREDITARY

OMIM:

 

610382

Gene summaries Genetic tests Medical literature