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Personalized Cause offers specialty pricing for Fundraising Events and Large Quantity Orders. Please give us a call at (949) 533-4977 or fill out the form to the right to request pricing. We offer reduced pricing on all Awareness Ribbon Pins and Personalized Awareness Ribbon Pins. Let us know how we can help. 

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949-533-4977

YOUR source for SINGLE custom awareness ribbons. Personalized awareness ribbons engraved with name, date, logo. Large selection of cancer ribbons.

Rare Diseases Awareness Ribbons - C | Personalized Cause

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

RARE DISEASES AND DISORDERS - C

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.

C syndrome
C-like syndrome
CADASIL
Cafe au lait spots multiple
Caffey disease
CAHMR syndrome
Calabro syndrome
Calcifying Epithelial Odontogenic Tumor
Calciphylaxis
Calcium Pyrophosphate Dihydrate Desposition Disease
California encephalitis
Calloso-genital dysplasia
Calvarial hyperostosis
Camera Marugo Cohen syndrome
Campomelia Cumming type
Campomelic dysplasia
Camptobrachydactyly
Camptocormism
Camptodactyly arthropathy coxa vara pericarditis syndrome
Camptodactyly joint contractures and facial skeletal dysplasia
Camptodactyly syndrome Guadalajara type 1
Camptodactyly syndrome Guadalajara type 2
Camptodactyly syndrome Guadalajara type 3
Camptodactyly taurinuria
Camptodactyly vertebral fusion
Camptodactyly fibrous tissue hyperplasia and skeletal dysplasia
Camptodactyly tall stature and hearing loss syndrome
Camptodactyly-ichthyosis syndrome
Camptomelic syndrome long limb type
Camurati Engelmann disease type 2
Camurati-Engelmann disease
Canavan disease
Candida glabrata
Candidiasis familial chronic mucocutaneous autosomal recessive
CANOMAD syndrome
Cantalamessa Baldini Ambrosi syndrome
Cantu Sanchez-Corona Fragoso syndrome
Cantu Sanchez-Corona Garcia-Cruz syndrome
Cantu Sanchez-Corona Hernandez syndrome
Capillary hemangioblastoma
Carbamoyl phosphate synthetase 1 deficiency
Carbon baby syndrome
Carcinoid syndrome
Carcinoid tumor
Carcinoid tumor childhood
Carcinoma of the vocal tract
Carcinoma of unknown primary site childhood
Cardiac diverticulum
Cardiac hydatid cysts with intracavitary expansion
Cardiac rupture
Cardiac valvular dysplasia X-linked
Cardioauditory syndrome of Sanchez Cascos
Cardiocranial syndrome
Cardioencephalomyopathy
Cardiofacial syndrome short limbs
Cardiofaciocutaneous syndrome
Cardiogenital syndrome
Cardiomelic syndrome Stratton Koehler type
Cardiomyopathy and deafness due to tRNA lysine gene mutation
Cardiomyopathy cataract hip spine disease
Cardiomyopathy diabetes deafness
Cardiomyopathy dilated with conduction defect type 1
Cardiomyopathy dilated with conduction defect type 2
Cardiomyopathy dilated with woolly hair and keratoderma
Cardiomyopathy due to anthracyclines
Cardiomyopathy hypogonadism collagenoma syndrome
Cardiomyopathy hypogonadism metabolic anomalies
Cardiomyopathy spherocytosis
Cardiomyopathy fatal fetal due to myocardial calcification
Cardioskeletal syndrome Kuwaiti type
Cardiospasm
Carnevale Hernandez Castillo syndrome
Carnevale syndrome
Carney complex
Carnitine palmitoyl transferase 1 deficiency
Carnitine palmitoyl transferase 2 deficiency
Carnitine palmitoyltransferase I deficiency muscle
Carnitine transporter deficiency
Carnitine-acyl-carnitine translocase deficiency
Carnosinemia
Caroli disease
Carotid body tumor
Carpal deformity migrognathia microstomia
Carpenter syndrome
Carpo tarsal osteolysis recessive
Carpotarsal osteochondromatosis
Carrington syndrome
Cartilage-hair hypoplasia
Cartilaginous cancer
Cartwright Nelson Fryns syndrome
Caspase-8 deficiency
Cassavism
Castleman's disease
Castro Gago Pombo Novo syndrome
Cat Eye syndrome
Cat scratch disease
Catamenial pneumothorax
Cataract and cardiomyopathy
Cataract and congenital ichthyosis
Cataract anterior polar dominant
Cataract ataxia deafness
Cataract congenital autosomal dominant
Cataract congenital dominant non nuclear
Cataract congenital Volkmann type
Cataract Hutterite type
Cataract hypertrichosis mental retardation
Cataract mental retardation hypogonadism
Cataract microcornea syndrome
Cataract microphthalmia septal defect
Cataract skeletal anomalies
Cataract alopecia sclerodactyly
Cataract autosomal recessive congenital 2
Cataract congenital with microcornea or slight microphthalmia
Cataract congenital with microphthalmia
Cataract microphthalmia and nystagmus
Cataract posterior polar 1
Cataract posterior polar 3
Cataract posterior polar 4
Cataract posterior polar 5
Cataract total congenital
Cataract zonular
Cataract-glaucoma
Cataract-microcephaly-failure to thrive-kyphoscoliosis
Cataracts ataxia short stature and mental retardation
Catastrophic antiphospholipid syndrome
Catatrichy
Catel Manzke syndrome
Caudal appendage deafness
Caudal duplication
Caudal regression syndrome
Cavernous lymphangioma
Cayler cardiofacial syndrome
Ccge syndrome
CD3 deficiency
CD4 deficiency
CDG syndrome type 3
CDG syndrome type 4
CDK4 linked melanoma
Cennamo Gangemi syndrome
Central centrifugal cicatricial alopecia
Central core disease
Central nervous system lymphoma primary
Central neurocytoma
Central post-stroke pain
Central serous chorioretinopathy
Cercarial Dermatitis
Cerebellar agenesis
Cerebellar astrocytoma childhood
Cerebellar ataxia and hypogonadotropic hypogonadism
Cerebellar ataxia ectodermal dysplasia
Cerebellar ataxia infantile with progressive external ophthalmoplegia
Cerebellar ataxia areflexia pes cavus optic atrophy and sensorinural hearing loss
Cerebellar degeneration
Cerebellar degeneration subacute
Cerebellar hypoplasia
Cerebellar hypoplasia tapetoretinal degeneration
Cerebellar hypoplasia with endosteal sclerosis
Cerebellar liponeurocytoma
Cerebello-olivary atrophy
Cerebelloparenchymal disorder 3
Cerebellum agenesis hydrocephaly
Cerebral astrocytoma childhood
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
Cerebral calcification cerebellar hypoplasia
Cerebral calcifications opalescent teeth phosphaturia
Cerebral cavernous malformation
Cerebral dysgenesis neuropathy ichthyosis and palmoplantar keratoderma syndrome
Cerebral folate deficiency
Cerebral gigantism jaw cysts
Cerebral palsy ataxic
Cerebral palsy athetoid
Cerebral palsy mixed
Cerebral palsy spastic diplegic
Cerebral palsy spastic hemiplegic
Cerebral palsy spastic monoplegic
Cerebral palsy spastic quadriplegic
Cerebral sarcoma
Cerebral sclerosis similar to Pelizaeus-Merzbacher disease
Cerebral ventricle cancer
Cerebro facio thoracic dysplasia
Cerebro-costo-mandibular syndrome
Cerebro-oculo-facio-skeletal syndrome
Cerebrocostomandibular-like syndrome
Cerebrospinal fluid leak
Cerebrotendinous xanthomatosis
Ceroid lipofuscinosis neuronal 1
Ceroid lipofuscinosis neuronal 10
Ceroid lipofuscinosis neuronal 2
Ceroid lipofuscinosis neuronal 3
Ceroid lipofuscinosis neuronal 4A autosomal recessive
Ceroid lipofuscinosis neuronal 4B autosomal dominant
Ceroid lipofuscinosis neuronal 5
Ceroid lipofuscinosis neuronal 6
Ceroid lipofuscinosis neuronal 7
Ceroid lipofuscinosis neuronal 8
Ceroid lipofuscinosis neuronal 9
Ceroid storage disease
Cerulean cataract
Cervical dystonia
Cervical hypertrichosis peripheral neuropathy
Cervical intraepithelial neoplasia
Cervical ribs Sprengel anomaly anal atresia and urethral obstruction
Chagas disease
Chanarin-Dorfman syndrome
Chancroid
Chandler's syndrome
CHANDS
Chang Davidson Carlson syndrome
Chaotic atrial tachycardia
Char syndrome
Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease deafness recessive type
Charcot-Marie-Tooth disease dominant intermediate 1
Charcot-Marie-Tooth disease dominant intermediate 2
Charcot-Marie-Tooth disease dominant intermediate 3
Charcot-Marie-Tooth disease neuronal type A
Charcot-Marie-Tooth disease neuronal type B
Charcot-Marie-Tooth disease neuronal type D
Charcot-Marie-Tooth disease type 1A
Charcot-Marie-Tooth disease type 1B
Charcot-Marie-Tooth disease type 1C
Charcot-Marie-Tooth disease type 1D
Charcot-Marie-Tooth disease type 1E
Charcot-Marie-Tooth disease type 1F
Charcot-Marie-Tooth disease type 2A
Charcot-Marie-Tooth disease type 2B
Charcot-Marie-Tooth disease type 2B1
Charcot-Marie-Tooth disease type 2B2
Charcot-Marie-Tooth disease type 2C
Charcot-Marie-Tooth disease type 2D
Charcot-Marie-Tooth disease type 2E
Charcot-Marie-Tooth disease type 2F
Charcot-Marie-Tooth disease type 2G
Charcot-Marie-Tooth disease type 2H
Charcot-Marie-Tooth disease type 2I
Charcot-Marie-Tooth disease type 2J
Charcot-Marie-Tooth disease type 2K
Charcot-Marie-Tooth disease type 4A
Charcot-Marie-Tooth disease type 4B1
Charcot-Marie-Tooth disease type 4B2
Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma
Charcot-Marie-Tooth disease type 4C
Charcot-Marie-Tooth disease type 4E
Charcot-Marie-Tooth disease with ptosis and parkinsonism
Charcot-Marie-Tooth disease with pyramidal features autosomal dominant
Charcot-Marie-Tooth disease X-linked 1
Charcot-Marie-Tooth disease X-linked recessive 2
Charcot-Marie-Tooth disease X-linked recessive 3
Charcot-Marie-Tooth type 1 aplasia cutis congenita
CHARGE syndrome
Charles Bonnet syndrome
Charlie M syndrome
Chediak-Higashi syndrome
Cheilitis glandularis
Chemke Oliver Mallek syndrome
Cherubism
Chester porphyria
Chiari malformation type 0 (zero)
Chiari malformation type 1
Chiari malformation type 2
Chiari malformation type 3
Chiari malformation type 4
Chiari-Frommel syndrome
Chikungunya
Chilaiditi syndrome
CHILD syndrome
Childhood disintegrative disorder
Childhood-onset cerebral X-linked adrenoleukodystrophy
Childhood-Onset Schizophrenia
Children's interstitial lung disease
Chitayat Meunier Hodgkinson syndrome
Chitty Hall Baraitser syndrome
Chitty Hall Webb syndrome
Cholecystitis
Cholemia familial
Cholera
Cholestasis intrahepatic of pregnancy
Cholestasis progressive familial intrahepatic 1
Cholestasis progressive familial intrahepatic 2
Cholestasis progressive familial intrahepatic 3
Cholestasis progressive familial intrahepatic 4
Cholestatic jaundice renal tubular insufficiency
Cholesteatoma
Cholesterol pneumonia
Chondroblastoma
Chondrocalcinosis 1
Chondrocalcinosis 2
Chondrocalcinosis due to apatite crystal deposition
Chondrodysplasia
Chondrodysplasia acromesomelic with genital anomalies
Chondrodysplasia Blomstrand type
Chondrodysplasia calcificans metaphysealis
Chondrodysplasia lethal recessive
Chondrodysplasia punctata 1 X-linked recessive
Chondrodysplasia punctata 2 X-linked dominant
Chondrodysplasia punctata Sheffield type
Chondrodysplasia punctata syndrome
Chondrodysplasia punctata with steroid sulfatase deficiency
Chondrodysplasia punctata humero-metacarpal type
Chondrodysplasia situs inversus imperforate anus polydactyly
Chondrodysplasia Grebe type
Chondrodystrophy
Chondroma
Chondrosarcoma
Chordoid glioma of the third ventricle
Chordoma
Chorea familial benign
Chorea minor
Chorea remitting with nystagmus and cataracts
Choreoacanthocytosis
Choreoacanthocytosis amyotrophic
Choriocarcinoma
Chorioretinal atrophy progressive bifocal
Chorioretinitis
Chorioretinopathy dominant form microcephaly
Choroid plexus calcification with mental retardation
Choroid plexus carcinoma
Choroid plexus cyst
Choroid plexus papilloma
Choroidal dystrophy central areolar
Choroideremia
Choroideremia hypopituitarism
Choroiditis
Christian Demyer Franken syndrome
Christian Johnson Angenieta syndrome
Christianson syndrome
Chromhidrosis
Chromomycosis
Chromophil renal cell carcinoma
Chromophobe renal cell carcinoma
Chromosomal triplication
Chromosome 1 monosomy 1p
Chromosome 1 monosomy 1q4
Chromosome 1 ring
Chromosome 1 uniparental disomy 1q12 q21
Chromosome 1q21.1 micro duplication
Chromosome 10 monosomy 10p
Chromosome 10 monosomy 10q
Chromosome 10 ring
Chromosome 10 trisomy 10p
Chromosome 10 uniparental disomy
Chromosome 10q partial trisomy
Chromosome 11 deletion 11p
Chromosome 11q partial deletion
Chromosome 11q trisomy
Chromosome 12 ring
Chromosome 12 12p trisomy
Chromosome 12 trisomy 12q
Chromosome 12p deletion
Chromosome 13 ring
Chromosome 13p duplication
Chromosome 13q deletion
Chromosome 13q trisomy
Chromosome 13q-mosaicism
Chromosome 14 ring
Chromosome 14 mosaic trisomy
Chromosome 14q partial deletions
Chromosome 14q proximal duplication
Chromosome 14q terminal deletion
Chromosome 15 ring
Chromosome 15 trisomy mosaicism
Chromosome 15q partial deletion
Chromosome 15q tetrasomy
Chromosome 15q trisomy
Chromosome 16 trisomy
Chromosome 16 trisomy 16p
Chromosome 16 uniparental disomy
Chromosome 16p13.3 deletion syndrome
Chromosome 16p13.3 duplication
Chromosome 16q trisomy
Chromosome 17 ring
Chromosome 17 deletion
Chromosome 17 trisomy 17p
Chromosome 17 trisomy 17q22
Chromosome 18 mosaic monosomy
Chromosome 18 ring
Chromosome 18 tetrasomy 18p
Chromosome 18 trisomy 18p
Chromosome 18 trisomy 18q
Chromosome 18p deletion syndrome
Chromosome 18q deletion syndrome
Chromosome 19 ring
Chromosome 19 trisomy 19q
Chromosome 19q13.11 deletion syndrome
Chromosome 1p36 deletion syndrome
Chromosome 1q deletion
Chromosome 1q21.1 duplication syndrome
Chromosome 2 duplication(2)(p13)(p21)
Chromosome 2 monosomy 2q
Chromosome 2 monosomy 2q24
Chromosome 2 trisomy 2p
Chromosome 2 trisomy 2q
Chromosome 20 ring
Chromosome 20 deletion 20p
Chromosome 20 duplication 20p
Chromosome 20 trisomy
Chromosome 21 monosomy
Chromosome 21 ring
Chromosome 21 tetrasomy 21q
Chromosome 21 uniparental disomy
Chromosome 22 mosaic monosomy
Chromosome 22 ring
Chromosome 22 trisomy mosaic
Chromosome 22 trisomy
Chromosome 22q deletion
Chromosome 3 duplication syndrome
Chromosome 3 monosomy 3p
Chromosome 3 trisomy 3p
Chromosome 3 trisomy 3q
Chromosome 3q29 microduplication syndrome
Chromosome 4 ring syndrome
Chromosome 4 short arm deletion
Chromosome 4 monosomy 4q
Chromosome 4 Trisomy 4p
Chromosome 4 trisomy 4q
Chromosome 5 trisomy 5p
Chromosome 5 trisomy 5q
Chromosome 5 uniparental disomy
Chromosome 6 ring syndrome
Chromosome 6 monosomy 6q
Chromosome 6 monosomy 6q2
Chromosome 6 trisomy 6p
Chromosome 6 trisomy 6q
Chromosome 7 ring syndrome
Chromosome 7 monosomy
Chromosome 7 partial monosomy 7p
Chromosome 7 trisomy 7p
Chromosome 7 trisomy 7q
Chromosome 7 trisomy mosaic
Chromosome 8 ring
Chromosome 8 monosomy 8p
Chromosome 8 monosomy 8p23 1
Chromosome 8 monosomy 8q
Chromosome 8 trisomy 8p
Chromosome 8 trisomy 8q
Chromosome 9 Ring
Chromosome 9 monosomy 9p
Chromosome 9 tetrasomy 9p
Chromosome 9 trisomy 9q
Chromosome 9p trisomy
Chronic active Epstein-Barr virus infection
Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature
Chronic berylliosis
Chronic demyelinizing neuropathy with IgM monoclonal
Chronic erosive gastritis
Chronic granulomatous disease
Chronic Infantile Neurological Cutaneous Articular syndrome
Chronic inflammatory demyelinating polyneuropathy
Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
Chronic lymphocytic leukemia
Chronic myeloid leukemia
Chronic myelomonocytic leukemia
Chronic myeloproliferative disorders
Chronic neutrophilic leukemia
Chronic polyradiculoneuritis
Chronic progressive external ophthalmoplegia
Chronic recurrent multifocal osteomyelitis
Chudley Rozdilsky syndrome
Chudley-Mccullough syndrome
Churg Strauss syndrome
Chylomicron retention disease
Chylothorax congenital
Chylous ascites
Cicatricial pemphigoid
Ciguatera fish poisoning
Ciliary discoordination due to random ciliary orientation
Ciliary dyskinesia with excessively long cilia
Ciliary dyskinesia due to transposition of ciliary microtubules
Ciliary dyskinesia-bronchiectasis
Cilliers Beighton syndrome
Circumscribed cutaneous aplasia of the vertex
Circumscribed disseminated keratosis Jadassohn Lew type
Citrulline transport defect
Citrullinemia type I
Clark-Baraitser syndrome
Clasped thumbs congenital
Classic Kaposi sarcoma
Clayton-Smith Donnai syndrome
Clear cell renal cell carcinoma
Cleft hand absent tibia
Cleft lip and palate malrotation cardiopathy
Cleft lip and/or palate with mucous cysts of lower
Cleft lip palate abnormal thumbs microcephaly
Cleft lip palate dysmorphism Kumar type
Cleft lip palate mental retardation corneal opacity
Cleft lip palate oligodontia syndactyly pili torti
Cleft lip palate pituitary deficiency
Cleft lip palate-tetraphocomelia
Cleft lower lip cleft lateral canthi chorioretinal
Cleft palate cardiac defect ectrodactyly
Cleft palate colobomata radial synostosis deafness
Cleft palate heart disease polydactyly absent tibia
Cleft palate lateral synechia syndrome
Cleft palate short stature vertebral anomalies
Cleft palate stapes fixation oligodontia
Cleft palate X-linked
Cleft palate midfacial hypoplasia triangular facies and sensorineural hearing loss
Cleft tongue syndrome
Cleft upper lip median cutaneous polyps
Cleidocranial dysplasia
Cleidocranial dysplasia recessive form
Cleidorhizomelic syndrome
Cloacal exstrophy
Clostridium difficile
Clostridium sordellii
Cluster headache
Cluttering
CMV antenatal infection
COACH syndrome
Coal worker's pneumoconiosis
Coarctation of aorta dominant
Coarse face hypotonia constipation
Coats disease
Cocaine antenatal infection
Coccidioidomycosis
Coccygodynia
Cochleosaccular degeneration of the inner ear and progressive cataracts
Cockayne syndrome
Cockayne syndrome type I
Cockayne syndrome type II
Cockayne syndrome type III
CODAS syndrome
Coenzyme Q cytochrome c reductase deficiency of
Coenzyme Q10 deficiency
Coffin syndrome 1
Coffin-Lowry syndrome
Coffin-Siris syndrome
Cogan's syndrome
Cogan-Reese syndrome
Cohen Hayden syndrome
Cohen Lockood Wyborney syndrome
Cohen syndrome
Cold agglutinin disease
Cold contact urticaria
Cole Carpenter syndrome
Collagenopathy type 2 alpha 1
Collagenous colitis
Collecting duct carcinoma
Collins Pope syndrome
Collins Sakati syndrome
Colloid cysts of third ventricle
Coloboma chorioretinal cerebellar vermis aplasia
Coloboma hair abnormality
Coloboma of alar-nasal cartilages with telecanthus
Coloboma of choroid and retina
Coloboma of eye lens
Coloboma of iris
Coloboma of lens ala nasi
Coloboma of macula
Coloboma of macula with type B brachydactyly
Coloboma of optic nerve
Coloboma of optic papilla
Coloboma porencephaly hydronephrosis
Coloboma cleft lip/palate and mental retardation syndrome
Colobomata unilobar lung heart defect
Colobomatous microphthalmia heart disease hearing
Colonic atresia
Colonic malakoplakia
Colorectal cancer childhood
Colpocephaly
Colver Steer Godman syndrome
Combarros Calleja Leno syndrome
Combined malonic and methylmalonic aciduria
Common variable immunodeficiency
Compartment syndrome
Complement component 2 deficiency
Complement component 8 deficiency type 1
Complement component 8 deficiency type 2
Complement component deficiency
Complement component receptor 1
Complement receptor deficiency
Complete atrioventricular canal
Complex regional pain syndrome
Conductive deafness malformed external ear
Cone dystrophy X-linked with tapetal-like sheen
Cone-rod dystrophy
Cone-rod dystrophy 1
Cone-rod dystrophy 2
Cone-rod dystrophy 3
Cone-rod dystrophy 5
Cone-rod dystrophy 6
Cone-rod dystrophy amelogenesis imperfecta
Cone-rod dystrophy X-linked 1
Cone-rod dystrophy X-linked 2
Cone-rod dystrophy X-linked 3
Congenital absence of the sternocleidomastoid muscle
Congenital adrenal hyperplasia
Congenital alopecia X-linked
Congenital amegakaryocytic thrombocytopenia
Congenital amputation
Congenital aneurysms of the great vessels
Congenital anosmia
Congenital antithrombin deficiency
Congenital antithrombin deficiency type 2
Congenital antithrombin deficiency type 3
Congenital aplastic anemia
Congenital arteriovenous shunt
Congenital articular rigidity
Congenital benign spinal muscular atrophy dominant
Congenital bilateral absence of the vas deferens
Congenital bronchobiliary fistula
Congenital cardiovascular shunt
Congenital central hypoventilation syndrome
Congenital chloride diarrhea
Congenital contractural arachnodactyly
Congenital contractures
Congenital craniosynostosis maternal hyperthyroiditis
Congenital cystic eye
Congenital cystic eye multiple ocular and intracranial anomalies
Congenital cytomegalovirus
Congenital diaphragmatic hernia
Congenital dislocation of the patella
Congenital disorder of glycosylation type 1A
Congenital disorder of glycosylation type 1B
Congenital disorder of glycosylation type 1C
Congenital disorder of glycosylation type 1D
Congenital disorder of glycosylation type 1E
Congenital disorder of glycosylation type 1F
Congenital disorder of glycosylation type 1G
Congenital disorder of glycosylation type 1H
Congenital disorder of glycosylation type 1I
Congenital disorder of glycosylation type 1J
Congenital disorder of glycosylation type 1K
Congenital disorder of glycosylation type 1L
Congenital disorder of glycosylation type 2A
Congenital disorder of glycosylation type 2B
Congenital disorder of glycosylation type 2C
Congenital disorder of glycosylation type 2D
Congenital disorder of glycosylation type 2E
Congenital disorder of glycosylation type 2G
Congenital disorder of glycosylation type I/IIX
Congenital disorders of glycosylation
Congenital dyserythropoietic anemia
Congenital dyserythropoietic anemia type 1
Congenital dyserythropoietic anemia type 2
Congenital dyserythropoietic anemia type 3
Congenital ectodermal dysplasia with hearing loss
Congenital fiber type disproportion
Congenital generalized fibromatosis
Congenital generalized lipodystrophy type 1
Congenital generalized lipodystrophy type 2
Congenital giant megaureter
Congenital heart block
Congenital heart disease ptosis hypodontia craniostosis
Congenital heart disease radio ulnar synostosis mental retardation
Congenital hemolytic anemia
Congenital hepatic fibrosis
Congenital herpes simplex
Congenital human immunodeficiency virus
Congenital hypomyelination neuropathy
Congenital hypothyroidism
Congenital hypotrichosis milia
Congenital ichthyosis microcephalus quadriplegia
Congenital ichtyosiform erythroderma
Congenital insensitivity to pain with hyperhidrosis
Congenital lipoid adrenal hyperplasia
Congenital megalo-ureter
Congenital mesoblastic nephroma
Congenital mitral malformation
Congenital mitral stenosis
Congenital mixovirus
Congenital mumps
Congenital Muscular dystrophy
Congenital muscular dystrophy syringomyelia
Congenital myasthenic syndrome with episodic apnea
Congenital myotonic dystrophy
Congenital nephrotic syndrome Finnish type
Congenital nonhemolytic jaundice
Congenital nonprogressive myopathy with Moebius and Robin sequences
Congenital porphyria
Congenital primary aphakia
Congenital pseudoarthrosis
Congenital pulmonary alveolar proteinosis
Congenital pulmonary lymphangiectasia
Congenital short femur
Congenital stenosis of cervical medullary canal
Congenital sucrase-isomaltase deficiency
Congenital sucrose isomaltose malabsorption
Congenital torticollis
Congenital tracheomalacia
Congenital unilateral pulmonary hypoplasia
Congenital vagal hyperreflexivity
Congenital varicella syndrome
Congenitally corrected transposition of the great arteries
Conjunctival melanoma
Conjunctivitis ligneous
Conjunctivitis with Pseudomembrane
Conn's syndrome
Connective tissue dysplasia Spellacy type
Conotruncal anomaly face syndrome
Conotruncal heart malformations
Continuous muscle fiber activity hereditary
Continuous spike-wave during slow sleep syndrome
Contractures ectodermal dysplasia cleft lip palate
Conversion disorder
Convulsions benign familial neonatal dominant form
Convulsions benign familial infantile 1
Copper deficiency familial benign
CoQ-responsive OXPHOS deficiency
Cor biloculare
Cor triatriatum
Cormier Rustin Munnich syndrome
Cornea guttata with anterior polar cataract
Corneal anesthesia deafness mental retardation
Corneal crystals myopathy neuropathy
Corneal dystrophy and perceptive deafness
Corneal dystrophy Avellino type
Corneal dystrophy crystalline of Schnyder
Corneal dystrophy Fuchs endothelial 1
Corneal dystrophy ichthyosis microcephaly mental retardation
Corneal dystrophy of Bowman layer type 1
Corneal dystrophy pigmentary anomaly malabsorption
Corneal dystrophy Thiel Behnke type
Corneal dystrophy lattice type 2
Corneal endothelial dystrophy type 2
Corneal hypesthesia familial
Cornelia de Lange syndrome
Corneodermatoosseous syndrome
Coronal synostosis syndactyly and jejunal atresia
Coronaro-cardiac fistula
Coronary arteries congenital malformation
Coronary artery aneurysm
Corpus callosum agenesis
Corpus callosum agenesis double urinary collecting
Corpus callosum agenesis of blepharophimosis Robin type
Corpus callosum agenesis polysyndactyly
Corpus callosum dysgenesis cleft spasm
Corpus callosum dysgenesis hypopituitarism
Corpus callosum dysgenesis X-linked recessive
Corsello Opitz syndrome
Cortada Koussef Matsumoto syndrome
Cortes Lacassie syndrome
Cortical blindness mental retardation polydactyly
Cortical defects wormian bones and dentinogenesis imperfecta
Cortical hyperostosis syndactyly
Corticobasal degeneration
Cortisone reductase deficiency
Costello syndrome
Costocoracoid ligament congenitally short
Cote Katsantoni syndrome
Cough headache
Cousin syndrome
Cowchock syndrome
Cowden's disease
Coxa vara congenital
Coxoauricular syndrome
Cramp-fasciculations syndrome
Crandall syndrome
Crane-Heise syndrome
Cranio osteoarthropathy
Cranioacrofacial syndrome
Craniodiaphyseal dysplasia
Craniodigital syndrome mental retardation
Cranioectodermal dysplasia
Craniofacial and skeletal defects
Craniofacial deafness hand syndrome
Craniofacial dysostosis arthrogryposis progeroid appearence
Craniofacial dysostosis with diaphyseal hyperplasia
Craniofacial dyssynostosis
Craniofacial dystonia
Craniofacial malformations asymmetric with polysyndactyly and abnormal skin and gut development
Craniofaciocardioskeletal syndrome
Craniofaciocervical osteoglyphic dysplasia
Craniofrontonasal dysplasia
Craniofrontonasal syndrome Teebi type
Craniometaphyseal dysplasia autosomal dominant
Craniometaphyseal dysplasia autosomal recessive type
Craniomicromelic syndrome
Craniopharyngioma
Craniorachischisis
Craniostenosis cataract
Craniostenosis with congenital heart disease mental retardation
Craniosynostosis
Craniosynostosis alopecia brain defect
Craniosynostosis arthrogryposis cleft palate
Craniosynostosis autosomal dominant
Craniosynostosis cleft lip palate arthrogryposis
Craniosynostosis contractures cleft
Craniosynostosis exostoses nevus epibulbar dermoid
Craniosynostosis Fontaine type
Craniosynostosis Maroteaux Fonfria type
Craniosynostosis mental retardation clefting syndrome
Craniosynostosis mental retardation heart defects
Craniosynostosis Philadelphia type
Craniosynostosis anal anomalies and porokeratosis
Craniosynostosis-mental retardation syndrome of Lin and Gettig
Craniotelencephalic dysplasia
Crawfurd syndrome
Creatine deficiency X-linked
Creeping myiasis
CREST syndrome
Cretinism athyreotic
Creutzfeldt-Jakob disease
Cri du chat syndrome
Crigler Najjar syndrome type 1
Crigler Najjar syndrome type 2
Crisponi syndrome
Crohn's disease of the esophagus
Crome syndrome
Cronkhite-Canada disease
Crossed polydactyly type 1
Crossed polysyndactyly
Crouzon syndrome
Crumpled helices and small mouth
Cryofibrinogenemia
Cryoglobulinemia
Cryoglobulinemia familial mixed
Cryopyrin-Associated Periodic syndromes (CAPS)
Cryptococcosis
Cryptogenic Organizing Pneumonia
Cryptomicrotia brachydactyly syndrome
Cryptophthalmos
Cryptorchidism arachnodactyly mental retardation
Cryptosporidiosis
Curly hair ankyloblepharon nail dysplasia syndrome
Curly hair-acral keratoderma-caries syndrome
Currarino triad
Cushing syndrome familial
Cushing's symphalangism
Cushing's syndrome
Cutaneous anthrax
Cutaneous larva migrans
Cutaneous lupus erythematosus
Cutaneous mastocytosis
Cutaneous necrotizing vasculitis
Cutaneous photosensitivity and colitis lethal
Cutaneous polyarteritis nodosa
Cutaneous sclerosis
Cutaneous T-cell lymphoma
Cutis Gyrata syndrome of Beare and Stevenson
Cutis gyratum acanthosis nigricans craniosynostosis
Cutis laxa
Cutis laxa osteoporosis
Cutis laxa autosomal dominant
Cutis laxa autosomal recessive type 1
Cutis laxa autosomal recessive type 2A
Cutis laxa autosomal recessive type 2B
Cutis marmorata telangiectatica congenita
Cutis verticis gyrata
Cutis verticis gyrata mental deficiency
Cutler Bass Romshe syndrome
Cyclic neutropenia
Cyclic thrombocytopenia
Cyclic vomiting syndrome
Cyclosporiasis
Cyprus facial neuromusculoskeletal syndrome
Cystic adenomatoid malformation of lung
Cystic fibrosis
Cystic hamartoma of lung and kidney
Cystic hygroma
Cystic hygroma lethal cleft palate
Cystic medial necrosis of aorta
Cysticercosis
Cystin transport protein defect of
Cystinosis
Cystinosis ocular nonnephropathic
Cystinuria
Cystinuria-lysinuria
Cystosarcoma phyllodes
Cytokine deficiency
Cytokine receptor deficiency
Cytomegalic inclusion disease
Cytomegalovirus retinitis
Cytoplasmic body myopathy
Czech dysplasia metatarsal type
Czeizel Losonci syndrome

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