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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 and Disorders Awareness Ribbons - P | Personalized Cause

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

RARE DISEASES AND DISORDERS - P


Pachydermoperiostosis
Pachygyria
Pachygyria with mental retardation and seizures
Pachygyria frontotemporal
Pachyonychia congenita
Pachyonychia congenita type 1
Pachyonychia congenita type 2
Pacman dysplasia
Paget disease of bone familial
Paget disease of the breast
Paget disease extramammary
Paget disease juvenile
PAGOD syndrome
Pagon Stephan syndrome
Paine syndrome
Palant cleft palate syndrome
Palatopharyngeal incompetence
Pallidopyramidal syndrome
Pallister W syndrome
Pallister-Hall syndrome
Pallister-Killian mosaic syndrome
Palmer Pagon syndrome
Palmoplantar keratoderma
Palmoplantar keratoderma of Sybert
Palmoplantar keratoderma epidermolytic
Pancreatic adenoma
Pancreatic beta cell agenesis with neonatal diabetes mellitus
Pancreatic cancer
Pancreatic cancer childhood
Pancreatic carcinoma familial
Pancreatic islet cell tumors
Pancreatic lipomatosis duodenal stenosis
Pancreatitis pediatric
Pancreatoblastoma
PANDAS
Panhypopituitarism X-linked
Panostotic fibrous dysplasia
Pantothenate kinase-associated neurodegeneration
Panuveitis
Papillary cystadenocarcinoma
Papillary eccrine adenoma
Papillary renal cell carcinoma
Papilledema
Papillon Lefevre syndrome
Papillorenal syndrome
Papular mucinosis
Papular urticaria
Paracoccidioidomycosis
Paraganglioma and gastric stromal sarcoma
Paragangliomas 1
Paragangliomas 2
Paragangliomas 3
Paragangliomas 4
Paragonimiasis
Parainfluenza virus type 3
Paralysis agitans juvenile of Hunt
Paramyotonia congenita
Paranasal sinus cancer adult
Paranasal sinus cancer childhood
Paraneoplastic cerebellar degeneration
Paraneoplastic Neurologic Disorders
Paraomphalocele
Paraplegia
Parapsoriasis
Paraquat lung
Parastremmatic dwarfism
Parathyroid cancer childhood
Parathyroid carcinoma
PARC syndrome
Parenchymatous cortical degeneration of cerebellum
Paris-Trousseau thrombocytopenia
Parkes Weber syndrome
Parkinson disease 3
Parkinson disease 9
Parkinson disease juvenile autosomal recessive
Parkinsonism early onset with mental retardation
Paroxysmal cold hemoglobinuria
Paroxysmal hemicrania
Paroxysmal nocturnal hemoglobinuria
Paroxysmal ventricular fibrillation
Parry Romberg syndrome
Pars planitis
Parsonage Turner syndrome
Partial agenesis of corpus callosum
Partial atrioventricular canal
Partial deletion of Y
Partial lissencephaly
Partington Anderson syndrome
Partington X-linked mental retardation syndrome
Parvovirus antenatal infection
Pashayan syndrome
Passos-Bueno syndrome
Pasteurella multocida infection
Patau syndrome
Patel Bixler syndrome
Patella aplasia coxa vara tarsal synostosis
Patella hypoplasia mental retardation
Patent ductus arteriosus
Patent ductus venosus
Patterned dystrophy of retinal pigment epithelium
Patterson pseudoleprechaunism syndrome
Patterson Stevenson syndrome
Pauciarticular chronic arthritis
Pearson marrow-pancreas syndrome
Pectus carinatum
Pediatric Crohns disease
Pediatric multiple sclerosis
Pediatric T-cell leukemia
Pediatric ulcerative colitis
Peeling skin syndrome
PEHO syndrome
Pelger-Huet anomaly
Pelizaeus-Merzbacher disease
Pelizaeus-Merzbacher disease late-onset type
Pellagra
Pellagra like syndrome
Pelvic dysplasia arthrogryposis of lower limbs
Pelvic lipomatosis
Pemphigoid gestationis
Pemphigus
Pemphigus and fogo selvagem
Pemphigus foliaceus
Pemphigus vulgaris
Pemphigus vulgaris familial
Pena Shokeir syndrome type 1
Pendred syndrome
Penile cancer adult
Penile cancer childhood
Penis agenesis
Penoscrotal transposition
Pentalogy of Cantrell
Pentosuria
Penttinen-Aula syndrome
PEPCK 1 deficiency
PEPCK 2 deficiency
Peptidic growth factors deficiency
Periarteritis nodosa
Pericardium absent mental retardation short stature
Perilymphatic fistula
Perimyositis
Periodic fever aphthous stomatitis pharyngitis and adenitis
Periodic fever familial autosomal dominant
Peripartum cardiomyopathy
Peripheral T-cell lymphoma
Peripheral type neurofibromatosis
Periventricular leukomalacia
Permanent neonatal diabetes mellitus
Perniosis
Peroxisome biogenesis disorders
Perry syndrome
Persistent hyperinsulinemic hypoglycemia of infancy
Persistent migraine aura without infarction (also known as "Visual Snow")
Persistent Mullerian duct syndrome
Persistent truncus arteriosus
Peters anomaly
Peters plus syndrome
Petit Fryns syndrome
Peutz Jeghers syndrome
Peyronie disease
Pfeiffer Kapferer syndrome
Pfeiffer Mayer syndrome
Pfeiffer Palm Teller syndrome
Pfeiffer Rockelein syndrome
Pfeiffer syndrome
Pfeiffer Tietze Welte syndrome
PHACE syndrome
Phacomatosis fourth
Phacomatosis pigmentokeratotica
Phacomatosis pigmentovascularis
PHAVER syndrome
Phelan-McDermid syndrome
Phenobarbital antenatal infection
Phenobarbital embryopathy
Phenothiazine antenatal infection
Phenylketonuria
Phenylketonuric embryopathy
Pheochromocytoma
Pheochromocytoma childhood
Pheochromocytoma-islet cell tumor syndrome
Philadelphia-negative chronic myeloid leukemia
Phocomelia contractures absent thumb
Phocomelia ectrodactyly deafness sinus arrhythmia
Phocomelia thrombocytopenia encephalocele
Phocomelia-ectrodactyly ear malformation deafness and sinus arrhythmia
Phosphoglucomutase deficiency
Phosphoglucomutase deficiency type 1
Phosphoglucomutase deficiency type 2
Phosphoglucomutase deficiency type 3
Phosphoglucomutase deficiency type 4
Phosphoglycerate kinase 1 deficiency
Phosphoglycerate kinase deficiency
Phosphomannoisomerase deficiency
Phosphoribosylpyrophosphate synthetase deficiency
Photosensitive epilepsy
Phyllodes tumor of the prostate
PIBIDS syndrome
Picardi-Lassueur-Little syndrome
Pick's disease
Piebaldism
Piepkorn Karp Hickok syndrome
Pierre Marie cerebellar ataxia
Pierre Robin sequence faciodigital anomaly
Pierre Robin sequence with pectus excavatum and rib and scapular anomalies
Pierre Robin syndrome skeletal dysplasia polydactyly
Pierre Robin's sequence
Pierson syndrome
Pigment-dispersion syndrome
Pigmentary retinopathy
Pigmented purpuric eruption Pigmented villonodular synovitis
Pili annulati
Pili multigemini
Pili torti
Pili torti developmental delay neurological abnormalities
Pili torti onychodysplasia
Pillay syndrome
Pilo dento ungular dysplasia microcephaly
Pilocytic astrocytoma
Pilodental dysplasia with refractive errors
Pilomatrixoma
Pilotto syndrome
Pineal parenchymal tumors of intermediate differentiation
Pineoblastoma
Pineoblastoma childhood
Pineocytoma
Pinheiro Freire-Maia Miranda syndrome
Pinta
Piriformis syndrome
Pitt syndrome
Pitt-Hopkins syndrome
Pituitary cancer
Pituitary dwarfism with large sella turcica
Pituitary hormone deficiency combined 1
Pituitary hormone deficiency combined 2
Pituitary hormone deficiency combined 3
Pituitary hormone deficiency combined 4
Pityriasis lichenoides
Pityriasis lichenoides chronica
Pityriasis lichenoides et varioliformis acuta
Pityriasis rubra pilaris
Piussan Lenaerts Mathieu syndrome
Placenta disorder
Plagiocephaly
Plagiocephaly and X-linked mental retardation
Plasma cell leukemia
Plasma thromboplastin antecedent deficiency
Plasmacytoma anaplastic
Plasmalogens synthesis deficiency isolated
Plasminogen activator inhibitor type 1 deficiency
Platelet disorder familial with associated myeloid malignancy
Platelet storage pool deficiency
Platyspondylic lethal skeletal dysplasia Torrance type
Pleoconial myopathy with salt craving
Pleomorphic malignant fibrous histiocytoma
Pleomorphic xanthoastrocytoma
Pleuropulmonary blastoma
Plexosarcoma
Plummer Vinson syndrome
Pneumocystic carinii pneumonia
Pneumocystosis
Pneumonia eosinophilic
Podder-Tolmie syndrome
POEMS syndrome
Poikiloderma with neutropenia
Poikilodermatomyositis mental retardation
Poikilodermia alopecia retrognathism cleft palate
Pointer syndrome
Poland syndrome
Poliomyelitis
Polyarteritis nodosa
Polyarthritis systemic
Polycystic bone disease
Polycystic kidneys severe infantile with tuberous sclerosis
Polycystic lipomembranous osteodysplasia with sclerosing
leukoencephalopathy
Polycystic liver disease
Polycythemia vera
Polydactyly
Polydactyly alopecia seborrheic dermatitis
Polydactyly cleft lip palate psychomotor retardation
Polydactyly myopia syndrome
Polydactyly postaxial
Polydactyly postaxial dental and vertebral
Polydactyly preaxial type 1
Polydactyly preaxial type 4
Polydactyly syndrome middle ray duplication
Polydactyly visceral anomalies cleft lip palate
Polyembryoma
Polyglucosan body disease adult
Polymicrogyria turricephaly hypogenitalism
Polymorphic catecholergic ventricular tachycardia
Polymorphic reticulosis
Polymorphous low-grade adenocarcinoma
Polymyositis
Polyneuropathy hand defect
Polyneuropathy mental retardation acromicria premature menopause
Polyomavirus allograft nephropathy
Polyosteolysis/hyperostosis syndrome
Polyostotic osteolytic dysplasia hereditary expansile
Polysyndactyly cardiac malformation
Polysyndactyly microcephaly ptosis
Polysyndactyly orofacial anomalies
Polysyndactyly trigonocephaly agenesis of corpus callosum
Polysyndactyly type 4
Polysyndactyly type Haas
Poncet-Spiegler's cylindroma
Pontocerebellar hypoplasia type 1
Pontocerebellar hypoplasia type 2
Pontocerebellar hypoplasia type 3
Pontocerebellar hypoplasia type 4
Pontocerebellar hypoplasia type 5
Pontocerebellar hypoplasia type 6
Pontoneocerebellar Hypoplasia
Popliteal pterygium syndrome
Popliteal pterygium syndrome lethal type
Porencephaly
Porencephaly cerebellar hypoplasia internal malformations
Porokeratosis of Mibelli
Porokeratosis plantaris palmaris et disseminata
Porokeratosis punctata palmaris et plantaris
Porokeratosis disseminated superficial actinic 1
Porokeratosis disseminated superficial actinic 2
Porphyria
Porphyria cutanea tarda
Portal hypertension
Portal hypertension due to infrahepatic block
Positive rheumatoid factor polyarthritis
Post Polio syndrome
Post-infectious myocarditis
Post-infectious reactive arthropathy
Post-Streptococcal Neurologic Disorders
Post-transplant lymphoproliferative disease
Post-traumatic epilepsy
Postaxial polydactyly mental retardation
Posterior column ataxia
Posterior column ataxia with retinitis pigmentosa
Posterior urethral valves
Posterior valve urethra
Postorgasmic illness syndrome
Postural orthostatic tachycardia syndrome
Potassium aggravated myotonia
Potato nose
Potocki-Lupski syndrome
Potocki-Shaffer syndrome
Potter syndrome
Potter syndrome type 1
Potter syndrome type 2
Potter syndrome type 3
Potter syndrome type 4
Powell Buist Stenzel syndrome
Prader-Willi habitus osteopenia and camptodactyly
Prader-Willi syndrome
Prata Libûral Gonûáalves syndrome
Preaxial deficiency postaxial polydactyly and hypospadias
Precocious epileptic encephalopathy
Precocious myoclonic encephalopathy
Precocious puberty
Precocious puberty gonadotropin-dependent
Preeyasombat Varavithya syndrome
Prekallikrein deficiency congenital
Premature aging Okamoto type
Premature atherosclerosis with photomyoclonic epilepsy deafness diabetes mellitus nephropathy an
Premature ovarian failure familial
Presenile dementia Kraepelin type
Priapism
Prieto X-linked mental retardation syndrome
Primary agammaglobulinemia
Primary amebic meningoencephalitis
Primary angiitis of the central nervous system
Primary basilar impression
Primary biliary cirrhosis
Primary carnitine deficiency
Primary ciliary dyskinesia
Primary cortisol resistance
Primary effusion lymphoma
Primary familial xanthomatosis with involvement and calcification of the adrenal galnds
Primary gastrointestinal melanoma
Primary hyperoxaluria type 1
Primary hyperoxaluria type 2
Primary hyperoxaluria type 3
Primary lateral sclerosis
Primary malignant lymphoma
Primary malignant melanoma of the cervix
Primary malignant melanoma of the conjunctiva
Primary open angle glaucoma juvenile onset 1
Primary orthostatic tremor
Primary progressive aphasia
Primary release disorder of platelets
Primary sclerosing cholangitis
Primary tubular proximal acidosis
Primrose syndrome
Prinzmetal's variant angina
Procarcinoma
Proconvertin deficiency congenital
Progeria
Progeria variant syndrome Ruvalcaba type
Progeroid short stature with pigmented nevi
Progeroid syndrome Petty type
Progeroid syndrome Penttinen type
Prognathism mandibular
Progressive black carbon hyperpigmentation of infancy
Progressive familial heart block type 1A
Progressive familial heart block type 1B
Progressive familial heart block type 2
Progressive hemifacial atrophy
Progressive kinking of the hair acquired
Progressive multifocal leukoencephalopathy
Progressive myoclonic epilepsy
Progressive non-fluent aphasia
Progressive osseous heteroplasia
Progressive Psuedorheumatoid Chondrodysplasia
Progressive supranuclear palsy
Progressive supranuclear palsy atypical
Progressive transformation of germinal centers
Prolactinoma familial
Prolerating trichilemmal cyst
Prolidase deficiency
Proopiomelanocortin deficiency
Properdin deficiency
Properdin deficiency X-linked
Propionic acidemia
Prosencephaly cerebellar dysgenesis
Prosopagnosia hereditary
Prosteglandin-Endoperoxide Synthase Deficiency
Prostatic malacoplakia associated with prostatic abscess
Prostatic stromal proliferation of uncertain malignant potential
Protein R deficiency
Protein S deficiency
Proteus like syndrome mental retardation eye defect
Proteus syndrome
Prothrombin thrombophilia
Protoporphyria
Proud Levine Carpenter syndrome
Proximal spinal muscular atrophy
Prune belly syndrome
Prurigo nodularis
Pruritic urticarial papules plaques of pregnancy
Pseudo Pelger-Huet anomaly
Pseudo-Turner syndrome
Pseudo-Von Willebrand disease
Pseudoachondroplasia
Pseudoachondroplastic dysplasia 2
Pseudoainhum
Pseudoaldosteronism
Pseudoaminopterin syndrome
Pseudoarylsulfatase A deficiency
Pseudocholinesterase deficiency
Pseudodiastrophic dysplasia
Pseudohermaphrodism anorectal anomalies
Pseudohyperkalemia Cardiff
Pseudohypoaldosteronism type 1 autosomal dominant
Pseudohypoaldosteronism type 1 autosomal recessive
Pseudohypoaldosteronism type 2
Pseudohypoparathyroidism
Pseudohypoparathyroidism type 1A
Pseudohypoparathyroidism type 1B
Pseudohypoparathyroidism type 1C
Pseudohypoparathyroidism type 2
Pseudoinflammatory fundus dystrophy
Pseudomarfanism
Pseudomonas stutzeri infections
Pseudomongolism
Pseudomyotonia
Pseudomyxoma peritonei
Pseudoneonatal adrenoleukodystrophy
Pseudopapilledema blepharophimosis hand anomalies
Pseudopelade of Brocq
Pseudopolycythaemia
Pseudoprogeria syndrome
Pseudopseudohypoparathyroidism
Pseudotrisomy 13 syndrome
Pseudotumor cerebri
Pseudovaginal perineoscrotal hypospadias
Pseudoxanthoma elasticum
Pseudoxanthoma elasticum dominant form
Pseudoxanthoma elasticum forme fruste
Pseudoxanthoma elasticum recessive form
Psittacosis
Pterigium Colli
Pterygia mental retardation and distinctive craniofacial features
Pterygium antecubital
Pterygium colli mental retardation digital anomalies
Pterygium of the conjunctiva and cornea
Ptosis coloboma mental retardation
Ptosis strabismus diastasis
Ptosis strabismus ectopic pupils
Pudendal Neuralgia
Pulmonar arterioveinous aneurysm
Pulmonary alveolar proteinosis acquired
Pulmonary arterio-veinous fistula
Pulmonary arteriovenous malformation
Pulmonary artery agenesis
Pulmonary artery coming from the aorta
Pulmonary artery familial dilatation
Pulmonary artery isolated unilateral absence of (Isolated UAPA)
Pulmonary artery unilateral absence of (UAPA)
Pulmonary atresia with ventricular septal defect
Pulmonary branches stenosis
Pulmonary edema of mountaineers
Pulmonary hypoplasia familial primary
Pulmonary sequestration
Pulmonary supravalvular stenosis
Pulmonary surfactant protein B deficiency of
Pulmonary valve stenosis
Pulmonary valves agenesis
Pulmonary vein stenosis
Pulmonary venoocclusive disease
Pulmonary venous return anomaly
Pulmonaryatresia intact ventricular septum
Pulmonic stenosis
Punctate acrokeratoderma freckle like pigmentation
Punctate inner choroidopathy
Pure autonomic failure
Pure red cell aplasia
Purine nucleoside phosphorylase deficiency
Pycnodysostosis
Pyknoachondrogenesis
Pyle disease
Pyoderma gangrenosum
Pyogenic arthritis pyoderma gangrenosum and acne
Pyomyositis
Pyridoxal 5'-phosphate-dependent epilepsy
Pyridoxine deficiency
Pyridoxine-dependent epilepsy
Pyropoikilocytosis hereditary
Pyruvate carboxylase deficiency
Pyruvate decarboxylase deficiency
Pyruvate dehydrogenase deficiency
Pyruvate dehydrogenase phosphatase deficiency
Pyruvate kinase deficiency
Pyruvate kinase deficiency liver type
Pyruvate kinase deficiency muscle type