Blue Jeans Awareness Ribbon for Rare Diseases as Designated by Global Genes®

Our Custom Blue Jeans awareness ribbons and non-personalized Blue Jeans awareness ribbons support this list of Rare Diseases as designated by Global Genes®. This list is extensive to include often under-funded, unknown diseases and disorders that need equal attention to those that receive a great deal of funding and recognition. Sometimes you will see a Rare Disease listed in two places on our website, and one may be associated with a color other than the Blue Jeans awareness ribbon. This is because often times a group has designated a color for a Rare Disease prior to the Blue Jeans awareness ribbon being designated for the entire category of causes.

Zebra Awareness Ribbons for Rare Diseases

Our custom zebra awareness ribbons and non-personalized zebra awareness ribbons also support our list of Rare Diseases. As you see on our site, rare diseases also use the blue denim ribbon. Prior to the use of blue jeans awareness ribbons, zebra awareness ribbons represented rare diseases. Rare diseases use a zebra stripe awareness ribbon because of the medical expression “When you hear hoof beats, think horses not zebras” in looking for a common diagnosis versus a rare one.

Our Rare Diseases and Disorders list is extensive to include often under-funded, unknown diseases and disorders that need equal attention to those that receive a great deal of funding and recognition. Sometimes you will see a Rare Disease listed in several places on our website, and one may be associated with a color other than the Blue Jeans awareness ribbon or the zebra awareness ribbon. This is because often times a group has designated a color for a Rare Disease itself rather than the entire category. Feel free to use the image or color that best reflects your efforts to raise awareness.

Galactokinase deficiency
Galactose epimerase deficiency
Gall bladder cancer
Game Friedman Paradice syndrome
Gamma aminobutyric acid transaminase deficiency
Gamma heavy chain disease
Gamma-cystathionase deficiency
Gangliosidosis generalized GM1 type 1
Gangliosidosis GM1 type 3
Gangliosidosis generalized GM1 type 2
GAPO syndrome
Gardner Morrison Abbot syndrome
Gardner syndrome
Gardner-Diamond syndrome
Garret Tripp syndrome
Gas bloat syndrome
Gastric duplication cysts
Gastric lymphoma
Gastro-enteropancreatic neuroendocrine tumor
Gastrocutaneous syndrome
Gastrointestinal Stromal Tumors
Gata1 Gene
Gaucher disease
Gaucher disease perinatal lethal
Gaucher disease type 1
Gaucher disease type 2
Gaucher disease type 3
Gaucher ichthyosis restrictive dermopathy
Gaucher-like disease
Gay Feinmesser Cohen syndrome
Gelatinous ascites
Geleophysic dwarfism
Gemignani syndrome
Genee-Wiedemann syndrome
Generalized dominant dystrophic epidermolysis bullosa
Generalized resistance to thyroid hormone
Generalized torsion dystonia
Genetic reflex epilepsy
Genital dwarfism
Genital dwarfism Turner type
Genito palato cardiac syndrome
Genoa syndrome
Genu valgum st Helena familial
Geographic tongue
German syndrome
Geroderma osteodysplasticum
Gershinibaruch Leibo syndrome
Gershoni-Baruch syndrome
Gerstmann syndrome
Gestational diabetes insipidus
Gestational trophoblastic tumor
Ghosal hematodiaphyseal dysplasia syndrome
Ghosal syndrome
Ghose Sachdev Kumar syndrome
Gianotti Crosti syndrome
Giant axonal neuropathy
Giant cell myocarditis
Giant congenital nevus
Giant ganglionic hyperplasia
Giant mammary hamartoma
Giant papillary conjunctivitis
Giant platelet syndrome
Gigantism advanced bone age hoarse cry
Gingival fibromatosis with distinctive facies
Gingival fibromatosis with hypertrichosis
Gingival fibromatosis 1
Gingival fibromatosis 2
Gingival fibromatosis 3
Gingival fibromatosis 4
Gitelman syndrome
Glanzmann thrombasthenia
Glass Chapman Hockley syndrome
Glassy cell carcinoma of the cervix
Glaucoma 3 primary infantile B
Glaucoma iridogoniodysgenesia
Glaucoma sleep apnea
Glaucoma type 1C
Glaucoma congenital
Glaucoma Ectopia Microspherophakia Stiff joints and Short stature syndrome
Glaucoma hereditary
Glaucoma hereditary adult type 1A
Glaucoma hereditary juvenile type 1B
Glaucoma primary infantile type 3A
Gliomatosis cerebri
Global disaccharide intolerance
Glomerulonephritis with sparse hair and telangiectases
Glomerulopathy with fibronectin deposits 1
Glomerulopathy with fibronectin deposits 2
Glomus jugulare tumors
Glomus tympanicum tumor
Glomus vagale tumors
Glossopalatine ankylosis micrognathia ear anomalies
Glossopharyngeal neuralgia
Glucagonoma syndrome
Glucocorticoid deficiency familial
Glucocorticoid resistance
Glucocorticoid-remediable aldosteronism
Glucose 6 phosphate dehydrogenase deficiency
Glucose transporter type 1 deficiency syndrome
Glucose-6-phosphate translocase deficiency
Glucose-galactose malabsorption
Glucosephosphate isomerase deficiency
Glucosidase acid-1 4-alpha deficiency
Glut2 deficiency
Glutamate decarboxylase deficiency
Glutamate formiminotransferase deficiency
Glutamine deficiency congenital
Glutaric acidemia type I
Glutaric acidemia type II
Glutathione synthetase deficiency
Glyceraldehyde-3-phosphate dehydrogenase deficiency
Glycine encephalopathy
Glycine N-methyltransferase deficiency
Glycogen storage disease 8
Glycogen storage disease type 0
Glycogen storage disease type 0 muscle
Glycogen storage disease type 12
Glycogen storage disease type 13
Glycogen storage disease type 1A
Glycogen storage disease type 1B
Glycogen storage disease type 2
Glycogen storage disease type 3
Glycogen storage disease type 4
Glycogen storage disease type 5
Glycogen storage disease type 6
Glycogen storage disease type 6 due to phosphorylation
Glycogen storage disease type 7
Glycosylphosphatidylinositol deficiency
GM2 gangliosidosis 0 variant
GM2-gangliosidosis B B1 AB variant
Gms syndrome
Gnathostoma Infection
Goblet cell carcinoma
Goldberg-Shprintzen megacolon syndrome
Goldenhar disease
Goldmann-Favre syndrome
Goldstein Hutt syndrome
Gollop Coates syndrome
Gollop syndrome
GOMBO syndrome
Gomez Lopez Hernandez syndrome
Gonadal dysgenesis
Gonadal dysgenesis mixed
Gonadal dysgenesis Turner type
Gonadal dysgenesis XY type associated anomalies
Gonadal dysgenesis XX type
Goniodysgenesis mental retardation short stature
Gonococcal conjunctivitis
Gonzales Del Angel syndrome
Good syndrome
Goodman syndrome
Goodpasture syndrome
Gordon syndrome
Gorlin Bushkell Jensen syndrome
Gorlin Chaudhry Moss syndrome
Gouty nephropathy familial
Gracile bone dysplasia
GRACILE syndrome
Graham Boyle Troxell syndrome
Grand Kaine Fulling syndrome
Grant syndrome
Granuloma annulare
Granuloma Inguinale
Granulomas congenital cerebral
Granulomatous Angiitis of the Central Nervous System
Granulomatous hypophysitis
Granulomatous rosacea
Granulosa cell tumor of the ovary
Graphite Pneumoconiosis
Graves' disease
Gray platelet syndrome
Green Sandford Davison syndrome
Greig cephalopolysyndactyly syndrome
Griscelli syndrome type 1
Griscelli syndrome type 2
Griscelli syndrome type 3
Grix Blankenship Peterson syndrome
Groenouw type I corneal dystrophy
Groll Hirschowitz syndrome
Grosse syndrome
Group B strep disease in newborns
Growth and mental retardation mandibulofacial dysostosis microcephaly and cleft palate
Growth deficiency brachydactyly unusual facies
Growth hormone deficiency
Growth hormone insensitivity with immunodeficiency
Growth mental deficiency syndrome of Myhre
Growth retardation alopecia pseudoanodontia optic
Growth retardation hydrocephaly lung hypoplasia
Growth retardation mental retardation phalangeal hypoplasia
Grubben de Cock Borghgraef syndrome
GTP cyclohydrolase I deficiency
Guanidinoacetate methyltransferase deficiency
Guillain-Barre syndrome
Guizar Vasquez Sanchez Manzano syndrome
Gupta Patton syndromev Gurrieri syndrome
Guttate psoriasis