Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/9
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- Pachyonychia congenita Jackson Lawler type
- Paes Whelan Modi syndrome
- Paget disease extramammary
- Paget disease juvenile type
- Pagon Bird Detter syndrome
- Pagon Stephan syndrome
- Pai Levkoff syndrome
- Palant cleft palate syndrome
- Palmer Pagon syndrome
- Palmitoyl-protein thioesterase deficiency
- Palmoplantar porokeratosis of Mantoux
- Pancreas agenesis
- Pancreatic adenoma
- Pancreatic beta cell agenesis with neonatal diabetes mellitus
- Pancreatic carcinoma, familial
- Pancreatic lipomatosis duodenal stenosis
- Pancreatitis, hereditary
- Panmyelophthisis aplastic anemia
- Panostotic fibrous dysplasia
- Papillion-Lefevre syndrome
- Papillitis
- Papilloma of choroid plexus
- Papular urticaria
- Parainfluenza virus type 3 antenatal infection
- Paramyotonia congenita of Von Eulenburg
- Paraparesis amyotrophy of hands and feet
- Paraplegia-brachydactyly-cone shaped epiphysis
- Paraplegia-mental retardation-hyperkeratosis
- Parastremmatic dwarfism
- Parathyroid neoplasm
- PARC syndrome
- Parenchymatous cortical degeneration of cerebellum
- Paris-Trousseau thrombopenia
- Parkes-Weber syndrome
- Parkinson dementia Steele type
- Parkinsonism early onset mental retardation
- Paroxysmal dystonic choreoathetosis
- Paroxysmal ventricular fibrillation
- Pars planitis
- Parsonage Turner syndrome
- Partial agenesis of corpus callosum
- Partial atrioventricular canal
- Partial deletion of Y
- Partial gigantism in context of NF
- Partial lissencephaly
- Partington Anderson syndrome
- Partington Mulley syndrome
- Parvovirus antenatal infection
- Pascuel Castroviejo syndrome
- Pashayan syndrome
- Pat1
- Pat11
- Pat111
- Pat12
- Pat121
- Pat13
- Pat131
- Pat132
- Pat14
- Pat141
- Pat142
- Patel Bixler syndrome
- Patella aplasia, coxa vara, tarsal synostosis
- Patella hypoplasia mental retardation
- Patent ductus arteriosus familial
- Patterson Lowry syndrome
- Patterson Stevenson syndrome
- Pauciarticular chronic arthritis
- Pavone Fiumara Rizzo syndrome
- Pearson's marrow/pancreas syndrome
- Peeling skin syndrome ichthyosis
- PEHO syndrome
- Pelizaeus-Merzbacher brain sclerosis
- Pelizaeus-Merzbacher disease, recessive, acute infantile
- Pelizaeus-Merzbacher leukodystrophy
- Pellagra like syndrome
- Pelvic dysplasia arthrogryposis of lower limbs
- Pelvic shoulder dysplasia
- Pemphigus and fogo selvagem
- Pemphigus vulgaris, familial
- Pena Shokeir syndrome
- Penis agenesia
- Penoscrotal transposition
- Penta X syndrome
- Penttinen-Aula syndrome
- PEPCK 1 deficiency
- PEPCK 2 deficiency
- PEPCK deficiency, mitochondrial
- Peptidic growth factors deficiency
- Pericardial constriction growth failure
- Pericardial defect diaphragmatic hernia
- Pericardium absent mental retardation short stature
- Pericardium congenital anomaly
- Perimyositis
- Periodic disease
- Peripheral blood vessel disorder
- Peripheral nervous disorder
- Peripheral neuroectodermal tumor
- Peripheral T-cell lymphoma
- Peripheral type neurofibromatosis
- Perisylvian syndrome
- Periventricular laminar heterotopia
- Perniola Krajewska Carnevale syndrome
- Peroxisomal Bifunctional Enzyme Deficiency
- Peroxisomal defects
- Persistent Mullerian duct syndrome (PMDS)
- Persistent parvovirus infection
- Peters anomaly with cataract
- Peters anomaly
- Peters congenital glaucoma
- Petit Fryns syndrome
- Petty Laxova Wiedemann syndrome
- Pfeiffer cardiocranial syndrome
- Pfeiffer Hirschfelder Rott syndrome
- Pfeiffer Kapferer syndrome
- Pfeiffer Mayer syndrome
- Pfeiffer Palm Teller syndrome
- Pfeiffer Rockelein syndrome
- Pfeiffer Singer Zschiesche syndrome
- Pfeiffer Tietze Welte syndrome
- Pfeiffer type acrocephalosyndactyly
- PHACE association
- Phacomatosis fourth
- Phacomatosis pigmentokeratotica
- Phacomatosis pigmentovascularis
- Pharyngeal plague
- Phenobarbital antenatal infection
- Phenobarbital embryopathy
- Phenol sulfotransferase deficiency
- Phenothiazine antenatal infection
- Phenylalanine hydroxylase deficiency
- Phenylalaninemia
- Phenylketonuria type II
- Phenylketonuric embryopathy
- Pheochromocytoma as part of NF
- Philadelphia-negative chronic myeloid leukemia
- Phocomelia contractures absent thumb
- Phocomelia ectrodactyly deafness sinus arrhythmia
- Phocomelia Schinzel type
- Phocomelia thrombocytopenia encephalocele
- Phosphate diabetes
- Phosphoenolpyruvate carboxykinase 1 deficiency
- Phosphoenolpyruvate carboxykinase 2 deficiency
- Phosphoenolpyruvate carboxykinase deficiency
- Phosphoglucomutase deficiency type 1
- Phosphoglucomutase deficiency type 2
- Phosphoglucomutase deficiency type 3
- Phosphoglucomutase deficiency type 4
- Phosphoglucomutase deficiency
- Phosphoglycerate kinase 1 deficiency
- Phosphoglycerate kinase deficiency
- Phosphomannoisomerase deficiency
- Phosphoribosylpyrophosphate synthetase deficiency
- Phytanic acid oxidase deficiency
- PIBIDS syndrome
- Picardi-Lassueur-Little syndrome
- Pie Torcido
- Piebald trait neurologic defects
- Piepkorn Karp Hickoc syndrome
- Pierre Marie cerbellar ataxia
- Pierre Robin sequence congenital heart defect talipes
- Pierre Robin sequence faciodigital anomaly
- Pierre Robin syndrome fetal chondrodysplasia
- Pierre Robin syndrome hyperphalangy clinodactyly
- Pierre Robin syndrome skeletal dysplasia polydactyly
- Pierre Robin's sequence
- Pigmentary retinopathy
- Pigment-dispersion syndrome
- Pignata guarino syndrome
- Pili canulati
- Pili torti developmental delay neurological abnormalities
- Pili torti nerve deafness
- Pili torti onychodysplasia
- Pillay syndrome
- Pilo dento ungular dysplasia microcephaly
- Pilotto syndrome
- Pinheiro Freire Maia Miranda syndrome
- Pinsky Di George Harley syndrome
- Pitt Hopkins syndrome
- Pitt-Rogers-Danks syndrome
- Pituitary dwarfism 1
- Piussan Lenaerts Mathieu syndrome
- Placenta disorder
- Placenta neoplasm
- Plagiocephaly X linked mental retardation
- Plasmacytoma anaplastic
- Plasmalogenes synthesis deficiency isolated
- Plasminogen activitor inhibitor type 1 deficiency, congenital
- Plasminogen deficiency, congenital
- Platyspondylic lethal chondrodysplasia
- Platyspondyly amelogenesis imperfecta
- Plexosarcoma
- Plum syndrome
- Podder-Tolmie syndrome
- Poikiloderma congenital with bullae Weary type
- Poikiloderma hereditary acrokeratotic Weary type
- Poikiloderma of Kindler
- Poikiloderma of Rothmund-Thomson
- Poikilodermatomyositis mental retardation
- Poikilodermia alopecia retrognathism cleft palate
- Pointer syndrome
- Polyarteritis
- Polyarthritis, systemic
- Polycystic kidney disease, adult type
- Polycystic kidney disease, infantile type
- Polycystic kidney disease, infantile, type I
- Polycystic kidney disease, recessive type
- Polycystic kidney disease, type 1
- Polycystic kidney disease, type 2
- Polycystic kidney disease, type 3
- Polycystic ovarian disease, familial
- Polycystic ovaries urethral sphincter dysfunction
- Polydactyly alopecia seborrheic dermatitis
- Polydactyly cleft lip palate psychomotor retardation
- Polydactyly myopia syndrome
- Polydactyly postaxial dental and vertebral
- Polydactyly postaxial with median cleft of upper lip
- Polydactyly postaxial
- Polydactyly preaxial type 1
- Polydactyly syndrome middle ray duplication
- Polydactyly visceral anomalies cleft lip palate
- Polyglucosan body disease, adult
- Polymicrogyria turricephaly hypogenitalism
- Polymorphic catecholergic ventricular tachycardia
- Polymorphic macular degeneration
- Polyneuropathy hand defect
- Polyneuropathy mental retardation acromicria prema
- Polyomavirus Infections
- Polyposis hamartomatous intestinal
- Polyposis skin pigmentation alopecia fingernail changes
- Polysyndactyly cardiac malformation
- Polysyndactyly microcephaly ptosis
- Polysyndactyly orofacial anomalies
- Polysyndactyly overgrowth syndrome
- Polysyndactyly trigonocephaly agenesis of corpus callosum
- Polysyndactyly type 4
- Polysyndactyly type Haas
- Poncet-Spiegler's cylindroma
- Pontoneocerebellar Hypoplasia
- Popliteal pterygium syndrome lethal type
- Porencephaly cerebellar hypoplasia malformations
- Porokeratosis of Mibelli
- Porokeratosis plantaris palmaris et disseminata
- Porokeratosis punctata palmaris et plantaris
- Porphyria, Ala-D
- Porphyria, congenital erythropoietic
- Porphyria, hereditary coproporphyria
- Portal hypertension due to infrahepatic block
- Portal thrombosis
- Portuguese type amyloidosis
- Positive rheumatoid factor polyarthritis
- Postaxial polydactyly mental retardation
- Posterior tibial tendon rupture
- Posterior valve urethra
- Post-infectious myocarditis
- Potassium aggravated myotonia
- Potter disease type 1
- Potter disease, type 3
- Potter sequence cleft cardiopathy
- Potter syndrome dominant type
- Powell Buist Stenzel syndrome
- Powell Chandra Saal syndrome
- Powell Venencie Gordon syndrome
- Prata Liberal Goncalves syndrome
- Preaxial deficiency postaxial polydactyly hypospadia
- Preaxial polydactyly colobomata mental retardation
- Precocious epileptic encephalopathy
- Precocious myoclonic encephalopathy
- Precocious puberty, gonadotropin-dependent
- Precocious puberty, male limited
- Preeyasombat Viravithya syndrome
- Prekallikrein deficiency, congenital
- Premature aging, Okamoto type
- Premature atherosclerosis photomyoclonic epilepsy
- Premature menopause, familial
- Prenatal infections
- Prieto Badia Mulas syndrome
- Prieur Griscelli syndrome
- Primary agammaglobulinemia
- Primary ciliary dyskinesia, 2
- Primary craniosynostosis
- Primary cutaneous amyloidosis
- Primary granulocytic sarcoma
- Primary malignant lymphoma
- Primary orthostatic tremor
- Primary tubular proximal acidosis
- Primerose syndrome
- Procarcinoma
- Progeria short stature pigmented nevi
- Progeria variant syndrome Ruvalcaba type
- Progeroid syndrome De Barsy type
- Progeroid syndrome Petty type
- Progeroid syndrome, Penttinen type
- Prognathism dominant
- Progressive acromelanosis
- Progressive black carbon hyperpigmentation of infancy
- Progressive diaphyseal dysplasia
- Progressive hearing loss stapes fixation
- Progressive kinking of the hair, acquired
- Progressive myositis ossificans
- Progressive osseous heteroplasia
- Progressive supranuclear palsy atypical
- Progressive systemic sclerosis
- Prolactinoma, familial
- Prolerating trichilemmal cyst
- Prosencephaly cerebellar dysgenesis
- Prostaglandin antenatal infection
- Prostatic malacoplakia associated with prostatic abscess
- Protein R deficiency
- Protein S acquired deficiency
- Proteus like syndrome mental retardation eye defect
- Prothrombin deficiency
- Protoporphyria
- Proud Levine Carpenter syndrome
- Proximal myotonic dystrophy
- Proximal spinal muscular atrophy
- Proximal tubulopathy diabetes mellitus cerebellar ataxia
- Pseudoachondroplastic dysplasia 1
- Pseudoachondroplastic dysplasia
- Pseudoadrenoleukodystrophy
- Pseudoaminopterin syndrome
- Pseudoarylsulfatase A deficiency
- Pseudo-Gaucher disease
- Pseudohermaphrodism anorectal anomalies
- Pseudohermaphroditism female skeletal anomalies
- Pseudohermaphroditism male with gynecomastia
- Pseudohermaphroditism mental retardation
- Pseudohypoaldosteronism type 1
- Pseudohypoaldosteronism type 2
- Pseudomarfanism
- Pseudomonas stutzeri infections
- Pseudomongolism
- Pseudoobstruction idiopathic intestinal
- Pseudopapilledema blepharophimosis hand anomalies
- Pseudo-Pelade of Brocq
- Pseudopolycythaemia
- Pseudoprogeria syndrome
- Pseudo-torch syndrome
- Pseudo-Turner syndrome
- Pseudoxanthoma elasticum, dominant form
- Pseudoxanthoma elasticum, recessive form
- Pseudo-Zellweger syndrome
- Pterigium Colli
- Pterygia mental retardation facial dysmorphism
- Pterygium colli mental retardation digital anomalies
- Pterygium syndrome antecubital
- Pterygium syndrome multiple dominant type
- Pterygium syndrome X linked
- Pterygium syndrome, multiple
- Ptosis coloboma mental retardation
- Ptosis coloboma trigonocephaly
- Ptosis strabismus diastasis
- Ptosis strabismus ectopic pupils
- Pulmonar arterioveinous aneurysm
- Pulmonary agenesis
- Pulmonary alveolar proteinosis, congenital
- Pulmonary arterio-veinous fistula
- Pulmonary artery agenesis
- Pulmonary artery coming from the aorta
- Pulmonary artery familial dilatation
- Pulmonary atresia with ventricular septal defect
- Pulmonary blastoma
- Pulmonary branches stenosis
- Pulmonary cystic lymphangiectasis
- Pulmonary Disease, Chronic Obstructive
- Pulmonary Hypertension, Secondary
- Pulmonary hypoplasia familial primary
- Pulmonary supravalvular stenosis
- Pulmonary surfactant protein B, deficiency of
- Pulmonary valves agenesis
- Pulmonary veins stenosis
- Pulmonary veno-occlusive disease
- Pulmonary venous return anomaly
- Pulmonaryatresia intact ventricular septum
- Punctate acrokeratoderma freckle like pigmentation
- Punctate inner choroidopathy
- Puretic syndrome
- Purtilo syndrome
- Pyknoachondrogenesis
- Pyle disease
- Pyridoxine deficit
- Pyrimidinemia familial
- Pyruvate decarboxylase deficiency
- Pyruvate kinase deficiency, liver type
- Pyruvate kinase deficiency, muscle type
- Qazi Markouizos syndrome
- Quebec platelet disorder
- Quinquaud's decalvans folliculitis
- Radial defect Robin sequence
- Radial hypoplasia, triphalangeal thumbs and hypospadias
- Radial ray agenesis
- Radial ray hypoplasia choanal atresia
- Radiation induced angiosarcoma of the breast
- Radiation induced meningioma
- Radiation leukemia
- Radiation related neoplasm /cancer
- Radiation syndromes
- Radiation-Induced Brachial Plexopathy
- Radiculomegaly of canine teeth congenital cataract
- Radio digito facial dysplasia
- Radio renal syndrome
- Radioulnar synostosis mental retardation hypotonia
- Radioulnar synostosis retinal pigment abnormalities
- Radio-ulnar synostosis type 1
- Radio-ulnar synostosis type 2
- Radius absent anogenital anomalies
- Rambam Hasharon syndrome
- Rambaud Galian syndrome
- Ramer Ladda syndrome
- Ramon Syndrome
- Ramos Arroyo Clark syndrome
- Rapp-Hodgkin syndrome
- Rasmussen Johnsen Thomsen syndrome
- Rasmussen subacute encephalitis
- Ray Peterson Scott syndrome
- Rayner Lampert Rennert syndrome
- Reactive attachment disorder of early childhood
- Reactive attachment disorder of infancy
- Reardon Hall Slaney syndrome
- Reardon Wilson Cavanagh syndrome
- Recurrent laryngeal papillomas
- Recurrent peripheral facial palsy
- Recurrent respiratory papillomatosis
- Reductional transverse limb defects
- Refractory anemia
- Refsum disease, infantile form
- Refsum Syndrome
- Reginato Shiapachasse syndrome
- Reifenstein Syndrome
- Reinhardt Pfeiffer syndrome
- Renal adysplasia dominant type
- Renal agenesis meningomyelocele mullerian defect
- Renal agenesis, bilateral
- Renal caliceal diverticuli deafness
- Renal dysplasia diffuse autosomal recessive
- Renal dysplasia diffuse cystic
- Renal dysplasia megalocystis sirenomelia
- Renal genital middle ear anomalies
- Renal hepatic pancreatic dysplasia Dandy Walker cyst
- Renal hypertension
- Renal rickets
- Renal tubular acidosis progressive nerve deafness
- Renal tubular acidosis, distal, autosomal dominant
- Renal tubular acidosis, distal, autosomal recessive
- Renal tubular acidosis, distal, type 3
- Renal tubular acidosis, distal, type 4
- Renal tubular acidosis, distal
- Renal tubular transport disorders inborn
- Renier Gabreels Jasper syndrome
- Renoanogenital syndrome
- Renoprival hypertension
- Resistance to LH (luteinizing hormone)
- Resistance to thyroid stimulating hormone
- Respiratory chain deficiency malformations
- Respiratory distress syndrome, Adult
- Respiratory distress syndrome, infant
- Retina disorder
- Retinal dysplasia X linked
- Retinal telangiectasia hypogammaglobulinemia
- Retinis pigmentosa deafness hypogenitalism
- Retinitis pigmentosa mental retardation deafness
- Retinitis pigmentosa-deafness
- Retinohepatoendocrinologic syndrome
- Retinopathy anemia CNS anomalies
- Retinopathy aplastic anemia neurological abnormalities
- Retinopathy pigmentary mental retardation
- Retinopathy, arteriosclerotic
- Retinopathy, diabetic
- Retinoschisis, juvenile
- Retinoschisis, X-linked
- Retroperitoneal liposarcoma
- Rett like syndrome
- Reynolds Neri Hermann syndrome
- Rhabditida Infections
- Rhabdomyomatous dysplasia cardiopathy genital anomalies
- Rhabdomyosarcoma 1
- Rhabdomyosarcoma 2
- Rhabdomyosarcoma, alveolar
- Rheumatoid vasculitis
- Rhizomelic dysplasia type Patterson Lowry
- Rhizomelic pseudopolyarthritis
- Rhizomelic syndrome
- Rhumatoid purpura
- Ribbing disease
- Richards-Rundle syndrome
- Richieri Costa Da Silva syndrome
- Richieri Costa Gorlin syndrome
- Richieri Costa Guion Almeida acrofacial dysostosis
- Richieri Costa Guion Almeida Cohen syndrome
- Richieri Costa Guion Almeida dwarfism
- Richieri Costa Guion Almeida Rodini syndrome
- Richieri Costa Montagnoli syndrome
- Richieri Costa Orquizas syndrome
- Richieri Costa Silveira Pereira syndrome
- Richieri-Costa Colletto Otto syndrome
- Rieger syndrome
- Right atrium familial dilatation
- Right ventricle hypoplasia
- Rigid mask like face deafness polydactyly
- Rigid spine syndrome
- Ringed hair disease
- Rivera Perez Salas syndrome
- Roberts Syndrome
- Robin sequence and oligodactyly
- Robinow Sorauf syndrome
- Robinson Miller Bensimon syndrome
- Roch-Leri mesosomatous lipomatosis
- Rodini Richieri Costa syndrome
- Rokitansky Kuster Hauser syndrome
- Rokitansky sequence
- Romberg hemi-facial atrophy
- Rombo syndrome
- Rommen Mueller Sybert syndrome
- Rosenberg Chutorian syndrome
- Rosenberg Lohr syndrome
- Roussy Levy hereditary areflexic dystasia
- Rowley-Rosenberg syndrome
- Roy Maroteaux Kremp syndrome
- Rozin Hertz Goodman syndrome
- Rubella virus antenatal infection
- Rubinstein Taybi like syndrome
- Rudd Klimek syndrome
- Rudiger syndrome
- Rutledge Friedman Harrod syndrome
- Ruvalcaba Churesigaew Myhre syndrome
- Ruvalcaba syndrome
- Ruvalcaba-Myhre syndrome
- Ruvalcaba-Myhre-Smith syndrome (BRR)
- Ruzicka Goerz Anton syndrome
