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Phone - 949-533-4977

Email - PersonalizedCause.Awareness@gmail.com

Sales & Orders - Sarah.PersonalizedCause@gmail.com

Fundraising and large quantity orders

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. 

Awareness Bracelets and Car Magnets available in quantities of 25+.

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 and Disorders Awareness Ribbons - N | Personalized Cause

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

RARE DISEASES AND DISORDERS - N


N acetyltransferase deficiency
N syndrome
N-acetyl glucosamine 6-sulfate sulfatase deficiency
N-acetyl-alpha-D-galactosaminidase deficiency type III
N-acetylglutamate synthetase deficiency
Nablus mask-like facial syndrome
NADH cytochrome B5 reductase deficiency
Naegeli syndrome
Nager acrofacial dysostosis
Naguib-Richieri-Costa syndrome
Nail dysplasia isolated congenital
Nail patella syndrome
Nakajo syndrome
Nakamura Osame syndrome
Nance-Horan syndrome
Narcolepsy
Narrow oral fissure short stature cone shaped epiphyses
Nasal cavity cancer childhood
Nasal polyposis familial
Nasodigitoacoustic syndrome
Nasopalpebral lipoma coloboma syndrome
Nasopharyngeal cancer childhood
Nasopharyngeal carcinoma
Natal teeth intestinal pseudoobstruction and patent ductus
Nathalie syndrome
Native American myopathy
Navajo neurohepatopathy
Navajo poikiloderma
Naxos disease
Necrotizing enterocolitis
Necrotizing fasciitis
Negative rheumatoid factor polyarthritis
Neisseria meningitidis
Nelson syndrome
Nemaline myopathy 1
Nemaline myopathy 2
Nemaline myopathy 3
Nemaline myopathy 4
Nemaline myopathy 5
Nemaline myopathy 6
NEMO mutation with immunodeficiency
Neonatal adrenoleukodystrophy
Neonatal hemochromatosis
Neonatal herpes
Neonatal hypothyroidism
Neonatal intrahepatic cholestasis caused by citrin deficiency
Neonatal meningitis
Neonatal onset multisystem inflammatory disease (NOMID)
Neonatal ovarian cyst
Neonatal progeroid syndrome
Neonatal stroke
Neonatal systemic lupus erythematosus
Nephrocalcinosis
Nephrogenic diabetes insipidus
Nephrogenic Systemic Fibrosis
Nephronophthisis 1
Nephronophthisis familial adult spastic quadriparesis
Nephropathic cystinosis
Nephropathy deafness hyperparathyroidism
Nephropathy familial with hyperuricemia
Nephrosclerosis
Nephrosis deafness urinary tract digital malformation
Nephrotic syndrome ocular anomalies
Nephrotic syndrome idiopathic steroid-resistant
Nerve sheath neoplasm
Netherton syndrome
Neu Laxova syndrome
Neuhauser Daly Magnelli syndrome
Neuhauser Eichner Opitz syndrome
Neural crest tumor
Neuroaxonal dystrophy renal tubular acidosis
Neuroaxonal dystrophy infantile
Neuroblastoma
Neurocutaneous melanosis
Neuroectodermal endocrine syndrome
Neuroendocrine carcinoma of the cervix
Neuroepithelioma
Neurofaciodigitorenal syndrome
Neuroferritinopathy
Neurofibroma
Neurofibromatosis
Neurofibromatosis type 1
Neurofibromatosis type 2
Neurofibromatosis type 3A
Neurofibromatosis type 3B
Neurofibromatosis type 4
Neurofibromatosis type 5
Neurofibromatosis type 6
Neurofibromatosis-Noonan syndrome
Neurofibromatosis-pheochromocytoma-duodenal carcinoid syndrome
Neurofibrosarcoma
Neurogenic diabetes insipidus
Neurogenic hypertension
Neuroleptic malignant syndrome
Neuroma biliary tract
Neuromyelitis optica spectrum disorder
Neuronal ceroid lipofuscinoses
Neuronal interstitial dysplasia
Neuronal intranuclear inclusion disease
Neuropathy ataxia retinitis pigmentosa syndrome
Neuropathy hereditary sensory and autonomic type 1
Neuropathy motor sensory type 2 deafness mental retardation
Neuropathy sensory spastic paraplegia
Neuropathy congenital with arthrogryposis multiplex
Neuropathy distal hereditary motor Jerash type
Neuropathy hereditary motor and sensory LOM type
Neuropathy hereditary motor and sensory Okinawa type
Neuropathy hereditary motor and sensory Russe type
Neurosyphilis
Neurotoxicity syndromes
Neutral lipid storage disease with myopathy
Neutropenia lethal congenital with eosinophilia
Neutropenia monocytopenia deafness
Neutrophil-specific granule deficiency
Neutrophilic dermatosis acute febrile
Nevi flammei familial multiple
Nevo syndrome
Nevoid basal cell carcinoma syndrome
New daily-persistent headache
Nguyen syndrome
Nicolaides Baraitser syndrome
Niemann-Pick disease
Niemann-Pick disease type B
Niemann-Pick disease type C1
Niemann-Pick disease type C2
Niemann-Pick disease type D
Nievergelt syndrome
Night blindness skeletal anomalies unusual facies
Night blindness congenital stationary
Nijmegen breakage syndrome
Nipah virus encephalitis
Noble Bass Sherman syndrome
Nocardiosis
Nodular melanoma
Nodular nonsuppurative panniculitis
Noma
Non functioning pancreatic endocrine tumor
Non-alcoholic steatohepatitis (NASH)
Non-dystrophic myotonic disorders
Non-Hodgkin lymphoma childhood
Non-Hodgkin lymphoma during pregnancy
Non-lissencephalic cortical dysplasia
Non-small cell lung cancer
Non-small cell lung cancer childhood
Nonaka myopathy
Nondystrophic myotonia
Nonmedullary thyroid carcinoma with or without cell oxyphilia
Nonseminomatous germ cell tumor
Nonsyndromic hereditary sensorineural hearing loss
Noonan syndrome PTPN11
Noonan syndrome KRAS
Noonan syndrome SOS1
Noonan syndrome RAF1
Noonan syndrome BRAF
Noonan syndrome MAP2K1
Noonan syndrome clinical
Noonan syndrome with mulitple letigines (formerly known as Leopard syndrome)
Noonan-like syndrome with loose anagen hair
Noonan-like/multiple giant cell lesion syndrome
Normokalemic periodic paralysis
Norrie disease
North Carolina macular dystrophy
Norum disease
Notalgia paresthetica
Nova syndrome
Novak syndrome
Nuchal bleb familial
Nystagmus 1 congenital X- linked
Nystagmus 2 congenital autosomal dominant
Nystagmus 3 congenital autosomal dominant
Nystagmus 4 congenital autosomal dominant
Nystagmus congenital motor autosomal recessive
Nystagmus hereditary vertical
Nystagmus myoclonic