Similar organisations to SLC6A1 CONNECT
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Epilepsy Research
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Bridge the Gap
SYNGAP1 Foundation is a legacy page dedicated to preserving the work and mission of our 100% charitable nonprofit in the USA, focused on #SYNGAP1 To serve, educate and fund research for families coping with the effects of SYNGAP mutations.
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Cure Ahc Foundation
Alternating Hemiplegia of Childhood (AHC) is a complex, ultra-rare neurological disease.
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Eleanor Kaplan Foundation Inc
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Alliance/Advocacy Organizations
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Trpm3 Foundation
Patient advocacy and support for those affected by #TRPM3 #ionchannel related disorders.
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Haystack Project Inc
We are committed to the Ultra Rare Disease Community.
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Shwachman-Diamond Syndrome Alliance Inc
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Fund Raising and/or Fund Distribution
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Tbc1D24 Foundation
Tbc1d24 foundation is a research organization and connecting site for caregivers, families, and those diagnosed with Tbc1d24 mutations.
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Medical Specialty Research
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Curemapk8Ip3 Foundation
Family support network for patients and their families affected by a gene mutation in MAPK8IP3 Page for individuals and families with gene variant MAPK8IP3 Improve the lives of patients and families affected by a MAPK8IP3 gene mutation by performing the following activities: raising community awareness of MAPK8IP3-Related Neurodevelopmental Disorder; facilitating research of MAPK8IP3-Related Neurodevelopmental and related Disorders; collecting and disseminating information and resources relating to MAPK8IP3-Related Neurodevelopmental and related Disorders; supporting those affected by MAPK8IP3-Related Neurodevelopmental and related Disorders; and any other charitable educational or scientific activities that are in furtherance of the Corporation's purposes.
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Specifically Named Diseases
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CTNNB1 Connect and Cure Inc
Connecting families, raising awareness, finding treatments and a cure for CTNNB1 Syndrome 🧬💛💙 https://t.
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