Broad CMG Cohort Form
This form serves to collect general information about your cohort prior to case entry. Providing this information can help prevent entry of cases that do not meet CMG criteria, saving your group’s time.

PLEASE FILL OUR THIS FORM SEPARATELY FOR EACH DISTINCT PHENOTYPE COHORT YOU ARE SUBMITTING (largely defined by genetic architecture). If you are proposing cases with many distinct phenotypes, then this form may not be appropriate and you should email with details.

Email address *
Submitter Name: *
Name of PI (if not submitter)
Name of research group: *
High level summary of disease: *
Ex. orphan disease, nephrotic syndrome, retinitis pigmentosa, brain malformations, neurodevelopmental, etc. (Space for a longer description of disease is located on page 3)
Has your group submitted cases to the Broad CMG before? *
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