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.

Fabry disease
FACES syndrome
Facial asymetry temporal seizures
Facial clefting corpus callosum agenesis
Facial dysmorphism shawl scrotum joint laxity syndrome
Facial ectodermal dysplasia
Facies unusual arthrogryposis advanced skeletal malformations
Facio digito genital syndrome recessive form
Facio skeletal genital syndrome Rippberger type
Facio thoraco genital syndrome
Faciocardiomelic dysplasia lethal
Faciocardiorenal syndrome
Faciomandibular myoclonus nocturnal
Facioscapulohumeral muscular dystrophy 1A
Factor 2 deficiency
Factor V deficiency
Factor VII deficiency
Factor X deficiency
Factor X deficiency congenital
Factor XI deficiency congenital
Factor XII deficiency
Factor XIII deficiency
Fairbank disease
Fallopian tube cancer
Fallot complex with severe mental and growth retardation
Fallot tetralogy
Familial adenomatous polyposis
Familial aortic dissection
Familial arteriosclerotic leukoencephalopathy alopecia lumbago without arterial hypertension
Familial band heterotopia
Familial bilateral striatal necrosis
Familial capillaro-venous leptomeningeal angiomatosis
Familial cold autoinflammatory syndrome
Familial colorectal cancer
Familial congenital fourth cranial nerve palsy
Familial cylindromatosis
Familial deafness
Familial dermographism
Familial dilated cardiomyopathy
Familial encephalopathy with neuroserpin inclusion bodies
Familial eosinophilia
Familial erythrocytosis 1
Familial exudative vitreoretinopathy
Familial hyperlipo-proteinemia type 1
Familial hypersecretion of adrenal androgens
Familial hypersensitivity pneumonitis
Familial hypertrophic cardiomyopathy
Familial hypocalciuric hypercalcemia
Familial hypocalciuric hypercalcemia type 1
Familial hypocalciuric hypercalcemia type 2
Familial hypocalciuric hypercalcemia type 3
Familial hypopituitarism
Familial hypothyroidism
Familial idiopathic basal ganglia calcification
Familial interstitial fibrosis
Familial Mediterranean fever
Familial multiple trichodiscomas
Familial myelofibrosis
Familial nasal acilia
Familial neurocardiogenic syncope
Familial non-immune hyperthyroidism
Familial opposable triphalangeal thumbs duplication
Familial partial paralysis
Familial periodic paralysis
Familial platelet disorder with associated myeloid malignancy
Familial porencephaly
Familial prostate cancer
Familial pulmonary arterial hypertension leucopenia and atrial septal defect
Familial renal cell carcinoma
Familial streblodactyly
Familial symmetric lipomatosis
Familial transthyretin amyloidosis
Familial Treacher Collins syndrome
Familial ventricular tachycardia
Familial Wilms tumor 2
Familial young-adult-onset arteriosclerotic
Fanconi anemia
Fanconi Bickel syndrome
Fanconi ichthyosis dysmorphism
Fanconi like syndrome
Fanconi renotubular syndrome
Fara Chlupackova syndrome
Farber's disease
Farmer's lung
Fatal familial insomnia
Fatal infantile encephalomyopathy
Fatty acid hydroxylase-associated neurodegeneration
Faulk Epstein Jones syndrome
Faye-Petersen Ward Carey syndrome
Fazio Londe syndrome
Febrile Ulceronecrotic Mucha-Habermann disease
Feigenbaum Bergeron Richardson syndrome
Feigenbaum Bergeron syndrome
Feingold Trainer syndrome
Felty's syndrome
Femoral facial syndrome
Femur bifid with monodactylous ectrodactyly
Femur fibula ulna syndrome
Fenton Wilkinson Toselano syndrome
Ferlini Ragno Calzolari syndrome
Fernhoff Blackston Oakley syndrome
Fertile eunuch syndrome
Fetal akinesia syndrome X-linked
Fetal Alcohol Spectrum Disorders
Fetal aminopterin syndrome
Fetal and neonatal alloimmune thrombocytopenia
Fetal antihypertensive drugs syndrome
Fetal brain disruption sequence
Fetal diethylstilbestrol syndrome
Fetal edema
Fetal enterovirus syndrome
Fetal hydantoin syndrome
Fetal indomethacin syndrome
Fetal iodine syndrome
Fetal left ventricular aneurysm
Fetal macrosomia
Fetal methimazole syndrome
Fetal methyl mercury syndrome
Fetal minoxidil syndrome
Fetal parainfluenza virus type 3 syndrome
Fetal parvovirus syndrome
Fetal phenothiazine syndrome
Fetal retinoid syndrome
Fetal thalidomide syndrome
Fetal valproate syndrome
Fetal warfarin syndrome
FG syndrome
FG syndrome 2
FG syndrome 3
FG syndrome 4
Fibrinogen deficiency congenital
Fibrocartilaginous embolism
Fibrodysplasia ossificans progressiva
Fibromatosis juvenile hyaline
Fibromatosis multiple non ossifying
Fibromuscular dysplasia
Fibrosing alveolitis
Fibrosing mediastinitis
Fibrous dysplasia
Fibula aplasia complex brachydactyly
Fibular aplasia
Fibular aplasia ectrodactyly
Fibular hypoplasia and complex brachydactyly
Fibular hypoplasia scapulo pelvic dysplasia absent
Filippi syndrome
Fine-Lubinsky syndrome
Finger locking recurrent with intrauterine growth retardation and proportionate short stature
Fish-eye disease
Fistulous vegetative verrucous hydradenoma
Fitz-Hugh-Curtis syndrome
Fitzsimmons syndrome
Fitzsimmons Walson Mellor syndrome
Fitzsimmons-Guilbert syndrome
Flat umbilicus familial
Flaujeac factor deficiency
Flavimonas oryzihabitans
Floating-Harbor syndrome
Florid cemento-osseous dysplasia
Florid cystic endosalpingiosis of the uterus
Florid papillomatosis of the nipple
FLOTCH syndrome
Flynn Aird syndrome
Focal alopecia congenital megalencephaly
Focal cortical dysplasia of Taylor
Focal dermal hypoplasia
Focal dystonia
Focal facial dermal dysplasia
Focal or multifocal malformations in neuronal migration
Foix Chavany Marie syndrome
Follicle-stimulating hormone deficiency isolated
Follicular dendritic cell tumor
Follicular lymphoma
Follicular lymphoreticuloma
Fontaine Farriaux Blanckaert syndrome
Forbes Albright syndrome
Formaldehyde poisoning
Forney Robinson Pascoe syndrome
Fountain syndrome
Fowler's syndrome
Fox-Fordyce disease
Fragile X syndrome
Fragile X syndrome type 1
Fragile X syndrome type 2
Fragile X syndrome type 3
Fragile XE syndrome
Fragoso Cid Garcia Hernandez syndrome
Franceschini Vardeu Guala syndrome
Franek Bocker kahlen syndrome
Frank Ter Haar syndrome
Fraser Jequier Chen syndrome
Fraser like syndrome
Fraser syndrome
Frasier syndrome
Freeman Sheldon syndrome
Freiberg's disease
Freire-Maia odontotrichomelic syndrome
Frenkel Russe syndrome
Frey's syndrome
Frias syndrome
Friedel Heid Grosshans syndrome
Friedman Goodman syndrome
Friedreich ataxia
Friedreich ataxia congenital glaucoma
Frints De Smet Fabry Fryns syndrome
Froelich syndrome
Fronto nasal malformation cloacal exstrophy
Frontofacionasal dysplasia
Frontometaphyseal dysplasia
Frontonasal dysplasia
Frontonasal dysplasia acromelic
Frontonasal dysplasia Klippel Feil syndrome
Frontonasal dysplasia phocomelic upper limbs
Frontotemporal dementia
Frontotemporal dementia ubiquitin-positive
Froster huch syndrome
Fructose-1 6-bisphosphatase deficiency
Fryns Fabry Remans syndrome
Fryns Hofkens Fabry syndrome
Fryns smeets thiry syndrome
Fryns syndrome
Fuchs atrophia gyrata chorioideae et retinae
Fuchs heterochromic iridocyclitis
Fucosidosis type 1
Fuhrmann syndrome
Fukuda Miyanomae Nakata syndrome
Fukuyama type muscular dystrophy
Fumaric aciduria
Functioning pancreatic endocrine tumor
Fundus dystrophy pseudoinflammatory of Sorsby
Fuqua Berkovitz syndrome
Furunculous myiasis
Fused mandibular incisors