• Birth Defects, Genetic Diseases

• 19.

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.

• Nonmonetary Support N.E.C.*

• 20.

Children of God for Life Inc

Established in 1999 with the goal of ending the exploitation of our unborn for profit.

LIV4THECURE

Liv4TheCure’s mission is to promote awareness, help families and fund research for Wolf Hirschhorn Syndrome.

• Fund Raising and/or Fund Distribution

• 22.

Childrens Rare Disease Organization Inc

Many children are living with a rare disease.

• Fund Raising and/or Fund Distribution

• 23.

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).

• Alliance/Advocacy Organizations

• 24.

Jansen De Vries Syndrome Foundation

The Jansen de Vries Syndrome (JdVS) Foundation is a nonprofit, tax-exempt organization as defined in section 501(c)(3) of the Internal Revenue Code and, as such, contributions to JdVS Foundation are tax-deductible.

• Public Foundations

• 25.

Orphan Disease Collective Inc

Funding research of rare diseases, supporeting promising work to develop treatments and cures.

• Fund Raising and/or Fund Distribution

• 26.

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.

• Diseases, Disorders, Medical Disciplines N.E.C.

• 27.

SIEGEL RARE NEUROIMMUNE ASSOCIATION

SRNA The nonprofit advocating for individuals with rare neuroimmune disorders ADEM AFM MOGAD NMOSD ON TM Help us provide hope and help to those living with ADEM AFM MOGAD NMOSD ON and TM.