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.

Saal Bulas syndrome
Sabinas brittle hair syndrome
Saccharopinuria
Sackey Sakati Aur syndrome
Sacral agenesis
Sacral defect with anterior meningocele
Sacral hemangiomas multiple congenital abnormalities
Sacral meningocele conotruncal heart defects
Sacral plexopathy
Sacrococcygeal Teratoma
Saethre-Chotzen syndrome
Saito Kuba Tsuruta syndrome
Sakati syndrome
Sakoda complex
Salcedo syndrome
Salivary gland cancer adult
Salivary gland cancer childhood
Salla disease
Sallis Beighton syndrome
Sammartino Decreccio syndrome
Samson Gardner syndrome
Samson Viljoen syndrome
Sanderson Fraser syndrome
Sandhaus Ben-Ami syndrome
Sandhoff disease
Sandifer syndrome
Santos Mateus Leal syndrome
SAPHO syndrome
Sarcoidosis
Sarcoma botryoides
Sarcosinemia
SARS
Satoyoshi syndrome
Saul Wilkes Stevenson syndrome
Say Barber Miller syndrome
Say Carpenter syndrome
Say Field Coldwell syndrome
Say Meyer syndrome
Say syndrome
Scalp defects postaxial polydactyly
Scalp ear nipple syndrome
Scaphotrapeziotrapezoid arthrodesis
Scapuloperoneal myopathy
Scapuloperoneal myopathy MYH7-related
Scapuloperoneal syndrome neurogenic Kaeser type
SCARF syndrome
Schaap Taylor Baraitser syndrome
Schaefer Stein Oshman syndrome
Scheuermann disease
Schimke immunoosseous dysplasia
Schimke X-linked mental retardation syndrome
Schindler disease type 1
Schinzel Giedion syndrome
Schisis association
Schistosomiasis
Schizencephaly
Schizophrenia mental retardation deafness retinitis
Schizotaxia
Schlegelberger Grote syndrome
Schmitt Gillenwater Kelly syndrome
Schneckenbecken dysplasia
Schnitzler syndrome
Scholte syndrome
Schrander-Stumpel Theunissen Hulsmans syndrome
Schroer Hammer Mauldin syndrome
Schwannoma
Schwannomatosis
Schwartz Cohen-Addad Lambert syndrome
Schwartz Jampel syndrome type 1
Scleredema
Scleroatonic muscular dystrophy
Sclerocornea Syndactyly ambiguous genitalia
Scleromyxedema
Sclerosing bone dysplasia mental retardation
Sclerosing mesenteritis
Sclerosteosis
Sclerotylosis
Scoliosis as part of NF
Scoliosis with unilateral unsegmented bar
SCOT deficiency
Scott Bryant Graham syndrome
Scott syndrome
Scurvy
Sea-Blue histiocytosis
Seaver Cassidy syndrome
Sebaceous gland hyperplasia familial presenile
Sebocystomatosis
Secernentea Infections
Seckel like syndrome Majoor-Krakauer type
Seckel syndrome
Secretory breast carcinoma
Sedlackova syndrome
Seemanova Lesny syndrome
Segawa syndrome autosomal recessive
Seghers syndrome
Segmental vertebral anomalies
Segmentation syndrome 1
Seizures benign familial neonatal recessive form
Seizures mental retardation hair dysplasia
Selective IgA deficiency
Selenium poisoning
Selig Benacerraf Greene syndrome
Semantic dementia
Seminoma
Semmekrot Haraldsson Weemaes syndrome
Sener syndrome
Senior Loken Syndrome
Sennetsu Fever
Sensory ataxic neuropathy dysarthria and ophthalmoparesis
Sensory neuropathy type 1
Senter syndrome
Seow Najjar syndrome
Sepiapterin reductase deficiency
Septo-optic dysplasia
Sequeiros Sack syndrome
Seres-Santamaria Arimany Muniz syndrome
Serkal syndrome
Serpentine fibula polycystic kidney syndrome
Serpiginous choroiditis
Sertoli cell-only syndrome
Sertoli-leydig cell tumors
SeSAME syndrome
Severe achondroplasia with developmental delay and acanthosis nigricans
Severe combined immunodeficiency
Severe combined immunodeficiency with sensitivity to ionizing radiation
Severe combined immunodeficiency atypical
Severe congenital neutropenia autosomal dominant
Severe congenital neutropenia autosomal recessive 3
Severe congenital neutropenia X-linked
Severe generalized recessive dystrophic epidermolysis bullosa
Severe immunodeficiency autosomal recessive T-cell negative B-cell negative NK cell-positive
Severe infantile axonal neuropathy
Severe mental retardation and absent nails of hallux and pollex
Sezary syndrome
Shapiro syndrome
Sharma Kapoor Ramji syndrome
Sharp syndrome
Shaver's disease
Sheehan syndrome
Shigellosis
Shith Filkins syndrome
Short bowel syndrome
Short broad great toe macrocranium
Short chain acyl CoA dehydrogenase deficiency
Short limb dwarf edema iris coloboma
Short limb dwarf lethal Colavita Kozlowski type
Short limb dwarf lethal Mcalister Crane type
Short limbs abnormal face congenital heart disease
Short limbs subluxed knees cleft palate
Short rib-polydactyly syndrome type 3
Short rib-polydactyly syndrome type 1
Short rib-polydactyly syndrome type 2
Short rib-polydactyly syndrome type 4
Short ribs craniosynostosis polysyndactyly
Short stature abnormal skin pigmentation mental retardation
Short stature contractures hypotonia
Short stature cranial hyperostosis hepatomegaly
Short stature deafness neutrophil dysfunction
Short stature dysmorphic face pelvic scapula dysplasia
Short stature hyperkaliemia acidosis
Short stature mental retardation eye anomalies
Short stature microcephaly seizures deafness
Short stature monodactylous ectrodactyly cleft palate
Short stature prognathism short femoral necks
Short stature Robin sequence cleft mandible hand anomalies clubfoot
Short stature syndrome Brussels type
Short stature talipes natal teeth
Short stature valvular heart disease
Short stature webbed neck heart disease
Short stature wormian bones dextrocardia
Short stature cranial hyperostosis hepatomegaly and diabetes
SHORT syndrome
Short tarsus absence of lower eyelashes
Shoulder and thorax deformity congenital heart disease
Shoulder girdle defect mental retardation familial
Shprintzen omphalocele syndrome
Shprintzen omphalocele syndrome
Shprintzen-Goldberg craniosynostosis syndrome
Shwachman-Diamond syndrome
Shwartzman phenomenon
Sialadenitis
Sialidosis type I
Sialidosis type II
Sialuria French type
Sickle cell anemia
Sickle delta beta thalassemia
Siderius X-linked mental retardation syndrome
Sideroblastic anemia acquired
Sideroblastic anemia and mitochondrial myopathy
Sideroblastic anemia pyridoxine-refractory autosomal recessive
Sideroblastic anemia pyridoxine-responsive autosomal recessive
Sideroblastic anemia X-linked
Siderosis
Siegler Brewer Carey syndrome
Signet ring cell carcinoma
Silengo Lerone Pelizza syndrome
Silicosiderosis
Silicosis
Sillence syndrome
Silver-Russell syndrome
Silvery hair syndrome
Simian B virus infection
Simosa cranio facial syndrome
Simpson-Golabi-Behmel syndrome
Sine scleroderma
Singh Chhaparwal Dhanda syndrome
Single upper central incisor
Single ventricular heart
Singleton Merten syndrome
Sinonasal undifferentiated carcinoma
Sinus cancer
Sinus node disease and myopia
Sirenomelia
Sitosterolemia
Situs inversus
Situs inversus totalis with cystic dysplasia of kidneys and pancreas
Sixth nerve palsy
Sjogren's syndrome juvenile secondary to autoimmune disease
Sjogren-Larsson syndrome
Sjogren-Larsson-like syndrome
Skeletal dysplasia orofacial anomalies
Skeletal dysplasia San Diego type
Skeleto cardiac syndrome with thrombocytopenia
Skin cancer non melanoma childhood
Skin fragility woolly hair syndrome
Slavotinek Pike Mills Hurst syndrome
Slti Salem syndrome
Small cell lung cancer childhood
Small cell lung cancer adult
Small intestine cancer
Small intestine cancer childhood
Small non-cleaved cell lymphoma
Smallpox
Smith Martin Dodd syndrome
Smith McCort dysplasia
Smith-Lemli-Opitz syndrome type 1
Smith-Lemli-Opitz syndrome type 2
Smith-Magenis syndrome
Sneddon syndrome
Snowflake vitreoretinal degeneration
Snyder Robinson syndrome
Soft tissue sarcoma
Soft tissue sarcoma childhood
Sohval Soffer syndrome
Somatostatinoma
Sommer Hines syndrome
Sommer Rathbun Battles syndrome
Sommer Young Wee Frye syndrome
Sondheimer syndrome
Sonoda syndrome
Sosby syndrome
Sotos syndrome
Sparse hair ptosis mental retardation
Spasmodic dysphonia
Spastic angina with healthy coronary artery
Spastic ataxia Charlevoix-Saguenay type
Spastic diplegia infantile type
Spastic paraparesis
Spastic paraparesis deafness
Spastic paraplegia 1
Spastic paraplegia 10
Spastic paraplegia 11
Spastic paraplegia 12
Spastic paraplegia 13
Spastic paraplegia 14
Spastic paraplegia 15
Spastic paraplegia 16
Spastic paraplegia 17
Spastic paraplegia 18
Spastic paraplegia 19
Spastic paraplegia 2
Spastic paraplegia 20
Spastic paraplegia 23
Spastic paraplegia 24
Spastic paraplegia 25
Spastic paraplegia 26
Spastic paraplegia 29
Spastic paraplegia 3
Spastic paraplegia 31
Spastic paraplegia 39
Spastic paraplegia 4
Spastic paraplegia 5A
Spastic paraplegia 5B
Spastic paraplegia 6
Spastic paraplegia 7
Spastic paraplegia 8
Spastic paraplegia 9
Spastic paraplegia and distal muscle wasting caused by neuropathy target esterase gene mutation
Spastic paraplegia epilepsy mental retardation
Spastic paraplegia facial cutaneous lesions
Spastic paraplegia nephritis deafness
Spastic paraplegia neuropathy poikiloderma
Spastic paraplegia with precocious puberty
Spastic paresis glaucoma mental retardation
Spastic quadriplegia retinitis pigmentosa mental retardation
Spasticity mental retardation
Spasticity multiple exostoses
Spellacy gibbs watts syndrome
Spermatogenesis arrest
Spheroid body myopathy
Sphingolipidosis
Spiegler-Brooke syndrome
Spielmeyer-Vogt-Sjogren-Batten disease
Spina bifida
Spina bifida hypospadias
Spinal atrophy ophthalmoplegia pyramidal syndrome
Spinal bulbar motor neuropathy
Spinal cord neoplasm
Spinal dysostosis type Anhalt
Spinal intradural arachnoid cysts
Spinal muscular atrophy
Spinal muscular atrophy 1
Spinal muscular atrophy Ryukyuan type
Spinal muscular atrophy type 1 with congenital bone fractures
Spinal muscular atrophy type 2
Spinal muscular atrophy type 3
Spinal muscular atrophy type 4
Spinal muscular atrophy with respiratory distress 1
Spinal shock
Spine rigid cardiomyopathy
Spinocerebellar ataxia
Spinocerebellar ataxia 1
Spinocerebellar ataxia 10
Spinocerebellar ataxia 11
Spinocerebellar ataxia 12
Spinocerebellar ataxia 13
Spinocerebellar ataxia 14
Spinocerebellar ataxia 15
Spinocerebellar ataxia 17
Spinocerebellar ataxia 18
Spinocerebellar ataxia 19
Spinocerebellar ataxia 2
Spinocerebellar ataxia 20
Spinocerebellar ataxia 21
Spinocerebellar ataxia 23
Spinocerebellar ataxia 25
Spinocerebellar ataxia 26
Spinocerebellar ataxia 27
Spinocerebellar ataxia 28
Spinocerebellar ataxia 29
Spinocerebellar ataxia 3
Spinocerebellar ataxia 30
Spinocerebellar ataxia 31
Spinocerebellar ataxia 4
Spinocerebellar ataxia 5
Spinocerebellar ataxia 6
Spinocerebellar ataxia 7
Spinocerebellar ataxia 8
Spinocerebellar ataxia 9
Spinocerebellar ataxia autosomal recessive 1
Spinocerebellar ataxia autosomal recessive 3
Spinocerebellar ataxia autosomal recessive 4
Spinocerebellar ataxia autosomal recessive 5
Spinocerebellar ataxia autosomal recessive 6
Spinocerebellar ataxia autosomal recessive with axonal neuropathy
Spinocerebellar ataxia with dysmorphism
Spinocerebellar ataxia X-linked type 2
Spinocerebellar ataxia X-linked type 3
Spinocerebellar ataxia X-linked type 4
Spinocerebellar degeneration and corneal dystrophy
Spinocerebellar degenerescence book type
Spirochetes disease
Spirurida Infections
Spitz nevus
Spleen neoplasm
Splenic infarcts
Splenogonadal fusion limb defects micrognatia
Splenomegaly
Split hand foot malformation
Split hand foot malformation 1
Split hand split foot malformation autosomal recessive
Split hand split foot mandibular hypoplasia
Split hand split foot nystagmus
Split hand urinary anomalies spina bifida
Split hand/foot malformation X-linked
Spondylarthropathy
Spondylocamptodactyly
Spondylocarpotarsal synostosis syndrome
Spondylocostal dysostosis 1
Spondylocostal dysostosis 2
Spondylocostal dysostosis 3
Spondylocostal dysostosis 4
Spondyloenchondrodysplasia
Spondyloepimetaphyseal dysplasia Genevieve type
Spondyloepimetaphyseal dysplasia joint laxity
Spondyloepimetaphyseal dysplasia Matrilin-3 related
Spondyloepimetaphyseal dysplasia micromelic
Spondyloepimetaphyseal dysplasia Missouri type
Spondyloepimetaphyseal dysplasia Shohat type
Spondyloepimetaphyseal dysplasia Sponastrime type
Spondyloepimetaphyseal dysplasia Strudwick type
Spondyloepimetaphyseal dysplasia with hypotrichosis
Spondyloepimetaphyseal dysplasia with multiple dislocations
Spondyloepimetaphyseal dysplasia X-linked
Spondyloepimetaphyseal dysplasia x-linked with mental deterioration
Spondyloepimetaphyseal dysplasia Aggrecan type
Spondyloepiphyseal dysplasia
Spondyloepiphyseal dysplasia congenita
Spondyloepiphyseal dysplasia Maroteaux type
Spondyloepiphyseal dysplasia Omani type
Spondyloepiphyseal dysplasia tarda autosomal dominant
Spondyloepiphyseal dysplasia tarda progressive arthropathy
Spondyloepiphyseal dysplasia tarda Toledo type
Spondyloepiphyseal dysplasia tarda X-linked
Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech
Spondylohypoplasia arthrogryposis and popliteal pterygium
Spondylometaepiphyseal dysplasia short limb-hand type
Spondylometaphyseal dysplasia Algerian type
Spondylometaphyseal dysplasia axial
Spondylometaphyseal dysplasia corner fracture type
Spondylometaphyseal dysplasia East-African type
Spondylometaphyseal dysplasia Kozlowski type
Spondylometaphyseal dysplasia Sedaghatian type
Spondylometaphyseal dysplasia type A4
Spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism
Spondylometaphyseal dysplasia with cone-rod dystrophy
Spondylometaphyseal dysplasia with dentinogenesis imperfecta
Spondylometaphyseal dysplasia X-linked
Spondyloperipheral dysplasia
Spondylospinal thoracic dysostosis
Spondylothoracic dysostosis
Spongiform encephalopathy
Spontaneous coronary artery dissection
Spontaneous periodic hypothermia
Spontaneous pneumothorax familial type
Sporotrichosis
Spotted fever
Spranger Schinzel Myers syndrome
Sprengel deformity
Squamous cell carcinoma of the head and neck
St Anthony's fire
Stachybotrys chartarum
Stalker Chitayat syndrome
Stampe sorensen syndrome
Staphylococcal food poisoning
Staphylococcal toxic shock syndrome
STAR syndrome
Stargardt disease
Stargardt macular degeneration absent or hypoplastic corpus callosum mental retardation and dysmorphic features
Status epilepticus
Steatocystoma multiplex
Steatocystoma multiplex with natal teeth
Steinfeld syndrome
Stenotrophomonas maltophilia
Sterility due to immotile flagella
Stern Lubinsky Durrie syndrome
Sternal cleft
Sternal cyst vascular anomalies
Sternal malformation vascular dysplasia association
Steroid dehydrogenase deficiency dental anomalies
Stevens-Johnson syndrome
Stewart Treves syndrome
Stickler syndrome
Stickler syndrome type 1
Stickler syndrome type 2
Stickler syndrome type 3
Stiff person syndrome
Stiff skin syndrome
Still's disease adult onset
Stocco dos Santos syndrome
Stoelinga de Koomen Davis syndrome
Stoll Alembik Dott syndrome
Stoll alembik finck syndrome
Stoll geraudel chauvin syndrome
Stoll kieny dott syndrome
Stomach cancer childhood
Stomach cancer familial
Stomach carcinoma
Stomatocytosis I
Stomatocytosis II
Storm syndrome
Stratton garcia young syndrome
Stratton Parker syndrome
Streptococcal Group A invasive disease
Streptococcal Group B invasive disease
Stress cardiomyopathy
Striatonigral degeneration infantile
Strongyloidiasis
Stuart factor deficiency congenital
Sturge-Weber syndrome
Stuve-Wiedemann syndrome
Subacute sclerosing panencephalitis
Subaortic stenosis short stature syndrome
Subcutaneous panniculitis-like T-cell lymphoma
Subependymal giant cell astrocytoma
Subependymal nodular heterotopia
Subependymoma
Subpulmonary stenosis
Subvalvular aortic stenosis
Succinic acidemia
Succinic acidemia lactic acidosis congenital
Succinic semialdehyde dehydrogenase deficiency
Succinyl-CoA acetoacetate transferase deficiency
Sudden Arrhythmia Death Syndrome
Sudden infant death syndrome
Sugarman brachydactyly
Sulfite oxidase deficiency
Summitt syndrome
SUNCT headache
Superficial siderosis of the central nervous system
Superficial spreading melanoma
Superior mesenteric artery syndrome
Superior vena cava syndrome
Supernumerary nipples
Supraglottic laryngeal cancer
Supranuclear ocular palsy
Supratentorial primitive neuroectodermal tumor
Supratentorial primitive neuroectodermal tumors childhood
Supraumbilical midabdominal raphe and facial cavernous hemangiomas
Susac syndrome
Sutton disease 2
Swyer James syndrome
Swyer syndrome
Sydenham's chorea
Symmastia
Symmetrical thalamic calcifications
Symphalangism brachydactyly
Symphalangism brachydactyly craniosynostosis
Symphalangism distal
Symphalangism familial proximal
Symphalangism short stature accessory testis
Symphalangism with multiple anomalies of hands and feet
Symphalangism distal with microdontia dental pulp stones and narrowed zygomatic arch
Syncamptodactyly scoliosis
Syndactyly cataract mental retardation

Syndactyly Cenani Lenz type
Syndactyly ectodermal dysplasia cleft lip palate hand foot
Syndactyly type 1
Syndactyly type 1 with cataracts and mental retardation
Syndactyly type 2
Syndactyly type 3
Syndactyly type 5
Syndactyly type 9
Syndactyly-polydactyly-earlobe syndrome
Syndesmodysplasic dwarfism
Syngnathia cleft palate
Syngnathia multiple anomalies
Synostoses tarsal carpal and digital
Synostosis of talus and calcaneus short stature
Synovial cancer
Synovial Chondromatosis
Synovial chondromatosis familial with dwarfism
Synovial sarcoma
Synovitis
Synovitis acne pustulosis hyperostosis osteitis
Syphilitic aseptic meningitis
Syphilitic myelopathy
Syringobulbia
Syringocystadenoma papilliferum
Syringomas natal teeth oligodontia
Syringomelia hyperkeratosis
Syringomyelia
Systemic candidiasis
Systemic capillary leak syndrome
Systemic mastocytosis
Systemic necrotizing angitis

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