Broad Center for Mendelian Genomics

GenCC Ref: GENCC:000115

Broad Center for Mendelian Genomics

This page is a summary of submissions provided by Broad Center for Mendelian Genomics. Click here to be notified about GenCC updates.

The Center for Mendelian Genomics at the Broad Institute of MIT and Harvard is a member of the GREGoR Consortium (Genomics Research to Elucidate the Genetics of Rare Disease) funded by the NHGRI (National Human Genome Research Institute), along with 5 other sites across the country. The central goals of the GREGoR consortium are: to discover variants and genes underlying Mendelian diseases; to collaboratively facilitate gene discovery, validation and follow up; and to generate new methods for improving diagnosis across a wide spectrum of rare disorders.


Website
Personnel
Christina Austin-Tse
Email: caustint@broadinstitute.org

Assertion Criteria

Submissions

30 total number of submissions
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Kleefstra syndrome 2
Submitted as: OMIM:617768
AD
04/01/2024
Evaluated
12/04/2024
Submitted
mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome
Submitted as: OMIM:617675
AR
04/01/2024
Evaluated
12/04/2024
Submitted
pontocerebellar hypoplasia type 2D
Submitted as: OMIM:613811
AR
04/01/2023
Evaluated
12/04/2024
Submitted
RNU4ATAC spectrum disorder
AR
08/16/2022
Evaluated
12/04/2024
Submitted
syndromic complex neurodevelopmental disorder
AD
04/01/2024
Evaluated
12/04/2024
Submitted
lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome
Submitted as: OMIM:617228
AR
11/22/2019
Evaluated
12/04/2024
Submitted
neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities
Submitted as: OMIM:618603
AD
09/01/2019
Evaluated
12/04/2024
Submitted
neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities
Submitted as: OMIM:619854
AD
11/05/2020
Evaluated
12/04/2024
Submitted
intellectual disability, X-linked 61
Submitted as: OMIM:300978
XL
11/12/2020
Evaluated
12/04/2024
Submitted
neurodevelopmental disorder with microcephaly and movement abnormalities
Submitted as: OMIM:620445
AR
03/06/2023
Evaluated
12/04/2024
Submitted
syndromic complex neurodevelopmental disorder
AD
05/01/2024
Evaluated
12/04/2024
Submitted
turnpenny-fry syndrome
Submitted as: OMIM:618371
AD
04/01/2024
Evaluated
12/04/2024
Submitted
hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome
Submitted as: OMIM:617915
AD
04/01/2024
Evaluated
12/04/2024
Submitted
pontocerebellar hypoplasia, type 14
Submitted as: OMIM:619301
AR
01/30/2019
Evaluated
12/04/2024
Submitted
neurodevelopmental disorder
AD
09/03/2019
Evaluated
12/04/2024
Submitted
neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum
Submitted as: OMIM:620250
AR
07/02/2024
Evaluated
12/04/2024
Submitted
neurodevelopmental disorder with hypotonia and brain abnormalities
Submitted as: OMIM:619512
AD
12/10/2018
Evaluated
12/04/2024
Submitted
intellectual developmental disorder 60 with seizures
Submitted as: OMIM:618587
AD
07/26/2024
Evaluated
12/04/2024
Submitted

The GenCC data are available free of restriction under a CC0 1.0 Universal (CC0 1.0) Public Domain Dedication. The GenCC requests that you give attribution to GenCC and the contributing sources whenever possible and appropriate. The accepted Flagship manuscript is now available from Genetics in Medicine (https://www.gimjournal.org/article/S1098-3600(22)00746-8/fulltext).

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