Search Results for: G

0-9• A• B• C• D• E• F• G• H• I• J• K• L• M• N• O• P• Q• R• S• T• U• V• W• X• Y• Z

Gastrointestinal Stromal Tumors

Gerstmann-Sträussler-Scheinker Disease

Giant Congenital Melanocytic Nevus

Glucose Transporter Type 1 Deficiency Syndrome

Glucose-6-Phosphate Dehydrogenase Deficiency

Glucose-Galactose Malabsorption

Glutathione Synthetase Deficiency

Glycogen Storage Disease Type I

Glycogen Storage Disease Type III

Glycogen Storage Disease Type IX

Glycogen Storage Disease Type V

Glycogen Storage Disease Type VII

Granulomatosis with Polyangiitis

Greig Cephalopolysyndactyly Syndrome

NORD's Rare Disease Database provides brief introductions for patients and their families to more than 1,200 rare diseases. This is not a comprehensive database since there are nearly 7,000 diseases considered rare in the U.S. We add new topics as we are able to do so, with the help of rare disease medical experts.

If you are seeking information about a rare disease that is not in this database, we would suggest contacting the Genetic and Rare Diseases Information Center (GARD) at the National Institutes of Health. NIH has the most complete database of rare diseases in the U.S.

Representatives of patient organizations whose medical advisors are interested in assisting NORD in creating a report on a disease not currently covered in this database may write to orphan@rarediseases.org.

Search Results for: G

Alone we are rare. Together we are strong.®