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.

T cell immunodeficiency primary
T-cell immunodeficiency congenital alopecia and nail dystrophy
T-cell lymphoma 1A
T-Lymphocytopenia
Tabatznik syndrome
Tachycardia hypertension microphthalmia and hyperglycinuria
Takayasu arteritis
Talipes equinovarus
Talo-patello-scaphoid osteolysis synovitis and short fourth metacarpals
Talonavicular coalition
Tang Hsi Ryu syndrome
Tangier disease
TAR syndrome
Tarlov cysts
TARP syndrome
Tarsal carpal coalition syndrome
Tarsal tunnel syndrome
TAU syndrome
Taurodontia absent teeth sparse hair
Taurodontism
Taurodontism microdontia and dens invaginatus
Tay Sachs disease
Teebi Kaurah syndrome
Teebi Naguib Al Awadi syndrome
Teebi Shaltout syndrome
Teebi syndrome
Teeth noneruption of with maxillary hypoplasia and genu valgum
Tel Hashomer camptodactyly syndrome
Telencephalic leukoencephalopathy
Telfer Sugar Jaeger syndrome
Temporal arteritis
Temporal epilepsy familial
Temporomandibular ankylosis
Temtamy preaxial brachydactyly syndrome
Temtamy syndrome
Tendons extensor of fingers anomalous insertion of
Teratoma
Testicular cancer
Testicular cancer childhood
Testotoxicosis
Tetanus
Tetra-amelia syndrome
Tetraamelia multiple malformations X-linked
Tetraamelia with ectodermal dysplasia and lacrimal duct abnormalities
Tetraamelia with pulmonary hypoplasia
Tetrahydrobiopterin deficiency
Tetralogy of fallot and glaucoma
Tetraploidy
Tetrasomy X
Thai symphalangism syndrome
Thakker Donnai syndrome
Thalamic degeneration symmetrical infantile
Thalamic degeneration symmetric infantile
Thalassemia
Thanatophoric dysplasia Glasgow variant
Thanatophoric dysplasia type 1
Thanatophoric dysplasia type 2
Theodor Hertz Goodman syndrome
Thiamine responsive megaloblastic anemia syndrome
Thickened earlobes with conductive deafness from incus-stapes abnormalities
Thin ribs tubular bones dysmorphism
Thiolase deficiency
Thiopurine S methyltranferase deficiency
Thomas Jewett Raines syndrome
Thomas syndrome
Thompson Baraitser syndrome
Thoracic celosomia
Thoracic dysplasia hydrocephalus syndrome
Thoracic outlet syndrome
Thoraco abdominal enteric duplication
Thoraco limb dysplasia Rivera type
Thoracolaryngopelvic dysplasia
Thoracomelic dysplasia
Thoracopelvic dysostosis
Thost-Unna palmoplantar keratoderma
Three M syndrome
Thrombasthenia
Thrombocytopathy asplenia miosis
Thrombocytopenia 2
Thrombocytopenia cerebellar hypoplasia short stature
Thrombocytopenia essential
Thrombocytopenia Robin sequence
Thrombocytopenia with elevated serum IgA and renal disease
Thrombocytopenia acquired amegakaryocytic
Thrombocytopenia x-linked
Thrombomodulin anomalies familial
Thrombotic thrombocytopenic purpura acquired
Thrombotic thrombocytopenic purpura congenital
Thumb absence hypoplastic halluces
Thumb absent short stature immune deficiency
Thumb deformity
Thumb deformity alopecia pigmentation anomaly
Thumb stiff brachydactyly mental retardation
Thunderclap headache
Thymic epithelial tumor
Thymic hyperplasia
Thymic-Renal-Anal-Lung dysplasia
Thymoma childhood
Thyrocerebral-retinal syndrome
Thyroglossal tract cyst
Thyroid agenesis
Thyroid cancer anaplastic
Thyroid cancer childhood
Thyroid cancer follicular
Thyroid cancer Hurthle cell
Thyroid cancer medullary
Thyroid hormone plasma membrane transport defect
Thyrotoxic periodic paralysis
Thyrotropin deficiency isolated
Tibia absent polydactyly arachnoid cyst
Tibiae bowed radial anomalies osteopenia fracture
Tibial aplasia ectrodactyly hydrocephalus
Tibial hemimelia cleft lip palate
Tick paralysis
Tick-borne encephalitis
Tiû?che-Jadassohn nevus
Tietz syndrome
Tietze syndrome
Tight skin contracture syndrome lethal
Tiglic acidemia
Togaviridae disease
Tollner Horst Manzke syndrome
Tolosa Hunt syndrome
Tome Brunet Fardeau syndrome
Tongue cancer
Toni-Debre-Fanconi syndrome
Toni-Fanconi syndrome
Tonoki syndrome
TORCH syndrome
Torg Winchester syndrome
Toriello Carey syndrome
Torsion dystonia
Torsion dystonia with onset in infancy
Torticollis keloids cryptorchidism renal dysplasia
Torticollis familial
Total Hypotrichosis Mari type
Touraine Solente Gole syndrome
Townes-Brocks syndrome
Toxic epidermal necrolysis
Toxocariasis
Trabecular fiber myopathy
Tracheal agenesis
Tracheal agenesis without tracheoesophageal fistula
Tracheobronchomalacia
Tracheobronchomegaly
Tracheobronchopathia osteoplastica
Tracheoesophageal fistula
Tracheoesophageal fistula symphalangism
Tracheophageal fistula hypospadias
Trachoma
Tranebjaerg Svejgaard syndrome
Transaldolase deficiency
Transcobalamin 1 deficiency
Transient Acantholytic Dermatosis
Transient bullous dermolysis of the newborn
Transient erythroblastopenia of childhood
Transient global amnesia
Transient neonatal arthrogryposis
Transitional cell carcinoma
Transposition of the great arteries
Transverse limb deficiency hemangioma
Transverse myelitis
Treacher Collins syndrome
Treft Sanborn Carey syndrome
Trehalase deficiency
Tremor hereditary essential 1
Tremor hereditary essential 2
Tremors nystagmus and duodenal ulcers
Treponema infection
Trichinosis
Tricho odonto onycho dermal syndrome
Tricho odonto onychodysplasia syndactyly dominant type
Tricho onychic dysplasia
Tricho onycho hypohidrotic dysplasia
Tricho retino dento digital syndrome
Tricho-dento-osseous syndrome
Tricho-dento-osseous syndrome 1
Tricho-hepato-enteric syndrome
Trichodental syndrome
Trichodermodysplasia dental alterations
Trichodysplasia xeroderma
Trichoepithelioma multiple familial 1
Trichoepithelioma multiple familial 2
Trichofolliculoma
Trichomalacia
Trichomegaly cataract hereditary spherocytosis
Trichomegaly with mental retardation dwarfism and pigmentary degeneration of retina
Trichoodontoonychial dysplasia
Trichorhinophalangeal syndrome type 1
Trichorhinophalangeal syndrome type 2
Trichorhinophalangeal syndrome type 3
Trichorrhexis nodosa syndrome
Trichoscyphodysplasia
Trichostasis spinulosa
Trichothiodystrophy nonphotosensitive
Trichothiodystrophy photosensitive
Trichotillomania
Trichuriasis
Tricuspid atresia
Trigeminal neuralgia
Trigger thumb
Trigonocephaly bifid nose acral anomalies
Trigonocephaly ptosis mental retardation
Trigonomacrocephaly tibial defect polydactyly
Trihydroxycholestanoylcoa oxidase isolated deficiency
Trimethylaminuria
Triopia
Triose phosphate-isomerase deficiency
Triphalangeal thumb non opposable
Triphalangeal thumb polysyndactyly syndrome
Triphalangeal thumbs brachyectrodactyly
Triple A syndrome
Triploidy
Trismus-pseudocamptodactyly syndrome
Trisomy 1 mosaicism
Trisomy 11 mosaicism
Trisomy 12 mosaicism
Trisomy 13
Trisomy 17 mosaicism
Trisomy 2 mosaicism
Trisomy 3 mosaicism
Trisomy 6
Trisomy 18 Chimerism, genetically displayed as XX/XY+18
Trochlea of the humerus aplasia of
Trochlear dysplasia
Trophoblastic tumor placental site
Tropical sprue
Trueb Burg Bottani syndrome
Trypanosomiasis Human East-African
Trypanosomiasis Human West-African
Tryptophanuria with dwarfism
Tsukahara Azuno Kajii syndrome
Tsukahara Kajii syndrome
Tuberculosis
Tuberculous meningitis
Tuberculous uveitis
Tuberous sclerosis
Tuberous sclerosis type 1
Tuberous sclerosis type 2
Tubulointerstitial nephritis and uveitis
Tucker syndrome
Tuffli Laxova syndrome
Tufted angioma
Tufted hair folliculitis
Tufting enteropathy
Tukel syndrome
Tularemia
Tumor Necrosis Factor Receptor-Associated Periodic syndrome (TRAPS)
Tungiasis
Tunglang Savage Bellman syndrome
Turcot syndrome
Turner syndrome
Twenty-nail dystrophy
Twin twin transfusion syndrome
Tylosis
Type 1 plasminogen deficiency
Typhoid fever
Typhus
Tyrosine-oxidase temporary deficiency
Tyrosinemia type 1
Tyrosinemia type 2
Tyrosinemia type 3

Source: globalgenes.org
Source: https://rarediseases.info.nih.gov/