Similar organisations to The Shank2 Foundation
-
Nerve, Muscle, and Bone Diseases
-
64.
Myotonic Dystrophy Foundation
The world's largest patient organization focused solely on #myotonicDystrophy.
8529
Oakland
-
Birth Defects, Genetic Diseases
-
65.
Gene Spotlight Inc
We are a nonprofit medical research and advocacy organization committed to spark breakthroughs in treatments and cures for rare genetic disorders, including lysosomal storage diseases, uncommon cancers and other orphan diseases.
MIAMI
-
Research Institutes and/or Public Policy Analysis
-
66.
Neurodegeneration Therapeutics Inc
CONDUCT BIOMEDICAL RESEARCH Neurodegeneration Therapeutics Inc NTI is 501c3 notforprofit biomedical research company that exists both to discover knowledge about the heterogeneity of adult brain diseases Alzheimers AD Parkinsons PD Lou Gherigs aka ALS and to develop novel personalized therapies for these disorders.
Crozet
Decoding Developmental Epilepsies
We serve two distinct communities. First, we serve those living with SCN8A and their families.
Washington
Beck Fahrner Syndrome Foundation
Our mission is to accelerate full spectrum research to cure Beck-Fahrner Syndrome (TET3 deficiency) and to empower affected families with information, knowledge, and connectivity.
Anoka
-
Fund Raising and/or Fund Distribution
-
69.
Arid1B Research Foundation
Accelerating the development of disease-modifying treatments for #ARID1B-RD (haploinsufficiency) - the most frequently mutated gene in de novo NDDs (ASD, ID).
677
Chevy Chase
-
Fund Raising and/or Fund Distribution
-
70.
Tbc1D24 Foundation
Tbc1d24 foundation is a research organization and connecting site for caregivers, families, and those diagnosed with Tbc1d24 mutations.
1600
Shohola
-
Patient Services�Entertainment, Recreation
-
71.
Idefine Inc
IDefine is committed to identifying life-changing treatments & cures and building community for those with Kleefstra Syndrome and intellectual disabilities.
1495
Atlanta
-
Fund Raising and/or Fund Distribution
-
72.
DHPS FOUNDATION
Leading the way in DHPS Deficiency Disorder research and education in order to find treatment, and a cure #curedhps #raredisease Our genetics make us unique our struggles and triumphs unite us.
98
RESTON





