Nonprofit OrganizationsBirth Defects & Genetic Diseases

MISSION:

HAPPY BREW PROVIDES EMPLOYMENT, TRAINING AND LEADERSHIP OPPORTUNITIES FOR INDIVIDUALS WITH INTELLECTUAL OR DEVELOPMENTAL DIFFERENCES IN THE COMMUNITY WHERE THEY ARE KNOWN, SEEN AND VALUED.

MISSION:

TURNER SYNDROME SOCIETY OF THE UNITED STATES (TSSUS) ADVANCES KNOWLEDGE, FACILITATES RESEARCH AND PROVIDES SUPPORT FOR ALL PERSONS TOUCHED BY TURNER SYNDROME.

MISSION:

THE MISSION OF SPINA BIFIDA ASSOCIATION OF CENTRAL FLORIDA IS TO PROMOTE THE PREVENTION OF SPINA BIFIDA AND TO ENHANCE THE LIVES OF ALL AFFECTED.

MISSION:

TO PROVIDE EDUCTION AND EMPOWERMENT CONCERNING THE TREATMENT OF BLEEDING DISORDERS.

MISSION:

The goal of this organization is to assiste in the prevention or treatment of illnesses or conditions that are hereditary and passed from parent to offspring. Use this code for organizations that focus on a wide variety of genetic disorders or on genetic disorders.

MISSION:

RADD IS THE TRUSTED PARTNER FOR YOUTH AND ADULTS WITH DEVELOPMENTAL DISABILITIES IN RACING COUNTY PROVIDING PROGRAMS FOR SOCIAL AND RECREATIONAL EXPERIENCES THAT IMPROVE THE LIVES OF INDIVIDUALS AND THEIR FAMILIES.

MISSION:

THE CHICAGO CF CARE SPECIALISTS NFP FOUNDATION IS COMMITTED TO THOSE AFFECTED BY CYSTIC FIBROSIS IN THE CHICAGOLAND AREA AND TO MAKING A DIFFERENCE BY BEING A MEANINGFUL AND ACTIVE SOURCE OF ASSISTANCE AND ADVOCACY FOR ALL CF INDIVIDUALS AND FAMILIES DEALING WITH THE EVERYDAY CHALLENGE OF CYSTIC FIBROSIS. THIS IS ACCOMPLISHED THROUGH CLINICAL RESEARCH, CLINICAL ASSISTANCE, AND EDUCATION.

MISSION:

TO CREATE AWARENESS IN THE DISORDERS ASSOCIATED WITH STXBP1 MUTATIONS. FUND AND DRIVE RESEARCH DISCOVERY OF A CURE. PROVIDE FAMILIES WITH TOOLS TO HELP THEM UNDERSTAND THE DISEASE & HOW TO GET INVOLVED. ADVOCATE TO IMPROVE EARLY DETECTION. FOSTER ACTIVISM TO HELP CHANGE POLICIES IN FAVOR OF ORPHANED DISEASES. IMPROVE THE LIVES OF OUR STXBP1 FAMILIES.

MISSION:

The goal of this organization is to assiste in the prevention or treatment of illnesses or conditions that are hereditary and passed from parent to offspring. Use this code for organizations that focus on a wide variety of genetic disorders or on genetic disorders.

MISSION:

TO FIND SPECIFIC TREATMENT OPTIONS AND A CURE FOR CACNA1A PATIENTS BY BUILDING A COLLABORATIVE NETWORK OF PATIENTS, FAMILIES, CLINICIANS AND SCIENTISTS THAT WILL WORK TOGETHER TO RAISE AWARENESS AND ACCELERATE THE UNDERSTANDING, DIAGNOSIS AND TREATMENT OF CACNA1A-LINKED DISEASES.

MISSION:

The goal of this organization is to assiste in the prevention or treatment of illnesses or conditions that are hereditary and passed from parent to offspring. Use this code for organizations that focus on a wide variety of genetic disorders or on genetic disorders.

MISSION:

THE PRIMARY EXEMPT PURPOSE IS TO PROVIDE MEDICATIONS, ENTERAL FORMULAS AND EQUIPMENT TO TREAT CYSTIC FIBROSIS PATIENTS AND OTHER CHRONICALLY ILL PATIENTS THAT SUFFER FROM RESPIRATORY, GASTROINTESTINAL, AND IMMUNOLOGIC DISEASES IRRREGARDLESS OF THEIR ABILITY TO PAY.

MISSION:

THE BOW FOUNDATION IS DEDICATED TO SUPPORTING GNAO1 FAMILIES, RESEARCH AND AWARENESS.

MISSION:

The goal of this organization is to assiste in the prevention or treatment of illnesses or conditions that are hereditary and passed from parent to offspring. Use this code for organizations that focus on a wide variety of genetic disorders or on genetic disorders.

MISSION:

The goal of this organization is to assiste in the prevention or treatment of illnesses or conditions that are hereditary and passed from parent to offspring. Use this code for organizations that focus on a wide variety of genetic disorders or on genetic disorders.

MISSION:

FOR COMMUNICATING AND PROVIDING ASSISTANCE TO CYSTIC FIBROSOS INDIVIDUALS AND THEIR FAMILIES

MISSION:

THE MISSION OF THE NETWORK IS TO PROMOTE XLH AWARENESS AND EDUCATION FOR AFFECTED FAMILIES, MEDICAL PROFESSIONALS, AND THE COMMUNITY AT LARGE.

MISSION:

PROMOTE RESEARCH OF CEREBRAL PALSY, SUPPORT PROGRAMS FOR MEDICAL TREATMENT, REHABILITATION, EDUCATION, AND SOCIAL NEEDS OF PEOPLE WITH CEREBRAL PALSY.

MISSION:

THE CORPORATION IS ORGANIZED TO PROVIDE ASSISTANCE AND SUPPORT TO THE NUECES CENTER FOR MENTAL HEALTH AND INTELLECTUAL DISABILITIES AS DEFINED IN IRS SECTION 509(A)(3).

MISSION:

EXPANDED RESEARCH AND DEVELOPES NEW WEBSITE TO DECIMINATE NEW INFORMATIONS AND RESEARCH ON THE TATTON BROWN RAHMAN SYNDROME.