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Rare Diseases Awareness Ribbons - D | Personalized Cause

Blue Jeans rare diseases awareness ribbons for rare diseases and disorders that begin with the letter D. Source: Global Genes®.

RARE DISEASES AND DISORDERS - D

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.

D ercole syndrome
D-2-alpha hydroxyglutaric aciduria
D-bifunctional protein deficiency
D-glycericacidemia
D-minus hemolytic uremic syndrome (D-HUS)
D-plus hemolytic uremic syndrome (D+HUS)
Daentl Towsend Siegel syndrome
Dahlberg Borer Newcomer syndrome
Daish Hardman Lamont syndrome
Dancing eyes-dancing feet syndrome
Dandy-Walker complex
Dandy-Walker cyst with Renal-Hepatic-Pancreatic dysplasia
Dandy-Walker like malformation with atrioventricular septal defect
Dandy-Walker malformation associated with macrocephaly facial anomalies developmental delay and brain stem dysgenesis
Dandy-Walker malformation with facial hemangioma
Dandy-Walker malformation with mental retardation basal ganglia disease and seizures
Dandy-Walker malformation with mental retardation macrocephaly myopia and brachytelephalangy
Dandy-Walker malformation with nasopharyngeal teratoma and diaphragmatic hernia
Dandy-Walker malformation with postaxial polydactyly
Dandy-Walker malformation with sagittal craniosynostosis and hydrocephalus
Daneman Davy Mancer syndrome
Danon disease
Darier disease
Dauwerse-Peters syndrome
Davenport Donlan syndrome
Davis Lafer syndrome
De Barsy syndrome
De Hauwere Leroy Adriaenssens syndrome
De Quervains' disease
De Sanctis-Cacchione syndrome
Deafness conductive ptosis skeletal anomalies
Deafness conductive stapedial ear malformation facial palsy
Deafness craniofacial syndrome
Deafness enamel hypoplasia nail defects
Deafness epiphyseal dysplasia short stature
Deafness goiter stippled epiphyses
Deafness hyperuricemia neurologic ataxia
Deafness hypogonadism syndrome
Deafness hypospadias metacarpal and metatarsal syndrome
Deafness mesenteric diverticula of small bowel neuropathy
Deafness mixed with perilymphatic Gusher X-linked
Deafness nephritis anorectal malformation
Deafness oligodontia syndrome
Deafness onychodystrophy dominant form
Deafness onychodystrophy osteodystrophy and mental retardation syndrome
Deafness peripheral neuropathy arterial disease
Deafness progressive cataract autosomal dominant
Deafness skeletal dysplasia lip granuloma
Deafness vitiligo achalasia
Deafness white hair contractures papillomas
Deafness with labyrinthine aplasia microtia and microdontia (LAMM)
Deafness X-linked DFN3
Deafness autosomal dominant nonsyndromic sensorineural 17
Deafness autosomal dominant nonsyndromic sensorineural 22
Deafness autosomal dominant nonsyndromic sensorineural 23
Deafness autosomal dominant nonsyndromic sensorineural 24
Deafness autosomal dominant nonsyndromic sensorineural 3
Deafness autosomal dominant nonsyndromic sensorineural 53
Deafness autosomal recessive 51
Deafness autosomal recessive 55
Deafness isolated due to mitochondrial transmission
Deafness neurosensory nonsyndromic recessive DFN
Deafness neurosensory autosomal recessive 47
Deafness progressive with stapes fixation
Deafness X-linked 2
Deafness X-linked DFN
Deal Barratt Dillon syndrome
Defective apolipoprotein B-100
Deficiency of interleukin-1 receptor antagonist
Degos 'en cocarde' erythrokeratoderma
Degos disease
Dehydrated hereditary stomatocytosis
Dehydrated hereditary stomatocytosis pseudohyperkalemia and perinatal edema
Delayed membranous cranial ossification
Delayed speech facial asymetry strabismus ear lobe creases
Delleman Oorthuys syndrome
Delta-1-pyrroline-5-carboxylate dehydrogenase deficiency
Delta-sarcoglycanopathy
Dementia familial British
Dementia familial Danish
Demodicidosis
Dengue fever
Dennis Fairhurst Moore syndrome
Dens in dente and palatal invaginations
Dent disease 1
Dent disease 2
Dentatorubral pallidoluysian atrophy
Dentin dysplasia sclerotic bones
Dentin dysplasia coronal
Dentin dysplasia type 1
Dentinogenesis imperfecta 1
Dentinogenesis imperfecta Shields type 3
Denys-Drash syndrome
Depersonalization disorder
Der Kaloustian Mcintosh Silver syndrome
Dermal eccrine cylindroma
Dermatitis herpetiformis familial
Dermatocardioskeletal syndrome Boronne type
Dermatofibroma
Dermatofibrosarcoma protuberans
Dermatoleukodystrophy
Dermatomyositis
Dermatoosteolysis Kirghizian type
Dermatopathia pigmentosa reticularis
Dermochondrocorneal dystrophy of Franûáois
Dermoids of cornea
Dermoodontodysplasia
Desbuquois syndrome
Desmoid disease hereditary
Desmoid tumor
Desmoplastic infantile astrocytoma
Desmoplastic infantile ganglioglioma
Desmoplastic small round cell tumor
Desmosterolosis
Developmental delay hypotonia extremities hypertrophy
Developmental dysphasia familial
Developmental dysplasia of hip
Devic disease
Devriendt syndrome
Dextrocardia
Dextrocardia with situs inversus
Dextrocardia with unusual facies and microphthalmia
Dextrocardia-bronchiectasis-sinusitis
DFNB1
Di Guglielmo's syndrome
Diabetes hypogonadism deafness mental retardation
Diabetes insipidus nephrogenic mental retardation and intracerebral calcification
Diabetes mellitus transient neonatal
Diabetes persistent mullerian ducts
Diabetes-deafness syndrome maternally transmitted
Diabetic mastopathy
Diamond-Blackfan anemia
Diamond-Blackfan anemia 2
Diamond-Blackfan anemia 3
Dianzani autoimmune lymphoproliferative syndrome
Diaphragmatic agenesis radial aplasia omphalocele
Diaphragmatic defect limb deficiency skull defect
Diaphragmatic hernia exomphalos corpus callosum agenesis
Diaphragmatic hernia upper limb defects
Diaphyseal medullary stenosis with malignant fibrous histiocytoma
Diastematomyelia
Diastrophic dysplasia
Dibasic aminoaciduria 1
Dibasic aminoaciduria 2
Dicarboxylic aminoaciduria
DICER1-related pleuropulmonary blastoma cancer predisposition syndrome
Die Smulders Droog Van Dijk syndrome
Die Smulders Vles Fryns syndrome
Diencephalic syndrome
Dieterich's disease
Diethylstilbestrol antenatal infection
Diffuse astrocytoma
Diffuse cavernous hemangioma of the rectum
Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia
Diffuse neonatal hemangiomatosis
Diffuse palmoplantar keratoderma Bothnian type
Diffuse panbronchiolitis
Diffuse scleroderma
Diffuse systemic sclerosis
DiGeorge syndrome
Digitorenocerebral syndrome
Dihydropteridine reductase deficiency
Dihydropyrimidine dehydrogenase deficiency
Dihydroxyadeninuria
Dilated cardiomyopathy
Dimauro disease
Dincsoy Salih Patel syndrome
Diomedi Bernardi Placidi syndrome
Dionisi Vici Sabetta Gambarara syndrome
Diphallia
Diphallus rachischisis imperforate anus
Diphosphoglycerate mutase deficiency of erythrocyte
Diphtheria
Diploid-triploid mosaicism
Diprosopia
Dipsogenic diabetes insipidus
Dissecting cellulitis of the scalp
Disseminated infection with mycobacterium avium complex
Distal arthrogryposis Moore Weaver type
Distal myopathy Markesbery-Griggs type
Distal myopathy with vocal cord weakness
Distal primary acidosis familial
Distichiasis heart congenital anomalies
Distomatosis
DK phocomelia syndrome
Dobrow syndrome
Dominant cleft palate
Dominant ichthyosis vulgaris
Donnai Barrow syndrome
Dopamine beta hydroxylase deficiency
Dosage-sensitive sex reversal
Double cortex syndrome
Double discordia
Double fingernail of fifth finger
Double nails on the fifth toe
Double outlet left ventricle
Double outlet right ventricle
Double tachycardia induced by catecholamines
Double uterus-hemivagina-renal agenesis
Dowling-Degos disease
Doxorubicin induced cardiomyopathy
Doyne honeycomb retinal dystrophy
Drachtman Weinblatt Sitarz syndrome
Dracunculiasis
Dravet syndrome
Duane anomaly mental retardation
Duane syndrome
Duane syndrome type 1
Duane syndrome type 2
Duane syndrome type 3
Duane-radial ray syndrome
Dubin-Johnson syndrome
Dubowitz syndrome
Duchenne muscular dystrophy
Duhring Brocq disease
Duker Weiss Siber syndrome
Duodenal atresia
Duodenal atresia tetralogy of Fallot
Duodenal ulcer due to antral G-cell hyperfunction
Duodenojejunal atresia with volvulus absent dorsal mesentery and absent superior mesenteric artery
Duplication of leg mirror foot
Duplication of the thumb unilateral biphalangeal
Duplication of urethra
Dupont Sellier Chochillon syndrome
Dupuytren subungual exostosis
Dwarfism bluish sclerae
Dwarfism deafness retinitis pigmentosa
Dwarfism familial with muscle spasms
Dwarfism lethal type advanced bone age
Dwarfism Levi type
Dwarfism stiff joint ocular abnormalities
Dwarfism tall vertebrae
Dwarfism thin bones multiple fractures
Dwarfism low-birth-weight type with unresponsiveness to growth hormone
Dwarfism mental retardation and eye abnormality
Dwarfism proportionate with hip dislocation
Dyggve-Melchior-Clausen syndrome
Dykes Markes Harper syndrome
Dysautonomia like disorder
Dyschondrosteosis nephritis
Dyschromatosis symmetrica hereditaria 1
Dyschromatosis universalis hereditaria
Dysembryoplastic neuroepithelial tumor
Dysequilibrium syndrome
Dysesthetic Vulvodynia
Dysferlinopathy
Dysfibrinogenemia
Dysgnathia complex
Dysharmonic skeletal maturation muscular fiber disproportion
Dyskeratosis congenita autosomal dominant
Dyskeratosis congenita autosomal recessive
Dyskeratosis congenita X-linked
Dyskinesia drug induced
Dysmorphism abnormal vocalization mental retardation
Dysmorphism cleft palate loose skin
Dysosteosclerosis
Dysostosis acral with facial and genital abnormalities
Dysostosis peripheral
Dysphasic dementia hereditary
Dysplasia epiphysealis hemimelica
Dysplastic cortical hyperostosis
Dysraphism cleft lip palate limb reduction defects
Dyssegmental dysplasia and glaucoma
Dyssegmental dysplasia Rolland-Desbuquois type
Dyssegmental dysplasia Silverman-Handmaker type
Dyssynergia cerebellaris myoclonica
Dystelephalangy
Dystonia 1
Dystonia 10
Dystonia 11
Dystonia 12
Dystonia 13
Dystonia 15 myoclonic
Dystonia 16
Dystonia 17
Dystonia 18
Dystonia 19
Dystonia 2 torsion autosomal recessive
Dystonia 3 torsion X-linked
Dystonia 4 torsion autosomal dominant type
Dystonia 5 Dopa-responsive type
Dystonia 6 torsion
Dystonia 7 torsion
Dystonia 8
Dystrophic epidermolysis bullosa
Dystrophinopathy

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