Center for Små Handicapgrupper er en selvejende institution underSocialministeriet og indgår i VISOs vidensfunktion under ServicestyrelsenCentret informerer og rådgiver både borgere og fagpersoner om sjældne handicap
Pallister-Killian Mosaic Syndrome
Pallister-Killian syndrom
PANDAS
Pantothenate kinase-associated neurodegeneration
Paroksystisk kinesigen dyskinesi (Familiær)
Paroxysmal kinesigenic choreoathetosis
Paroxysmal nocturnal hemoglobinuria
Paroxysmal tonic upgaze
Paroxystisk nocturn hæmoglobinuri
Parry Romberg Syndrom
Patau syndrom
Pearson marrow-pancreas syndrome
Pearsons syndrom
Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcus infections
Pelizaeus-Merzbacher sygdom
Pena Shokeir syndrom type 2
Pena-Shokeir syndrom, type 1
Pendred syndrom
Periodisk paralyse
Perisylvian Polymicrogyria
Perisylvian syndrom
Peroxisomal biogenese sygdomme
Peutz-Jegher syndrom
PFFD
PGA1
PHACE syndrom
Phaces association
Phelan-McDermid Syndrom
Phenylketonuria
PHS
Pierre Robin Sequence
Pierre-Robin syndrom
Pigmentnældefeber
Pitt Hopkins syndrom
PKU (Phenylketonuria)
Pletskaldethed
PNH
Poikiloderma atrophicans
Poikiloderma of Kindler
Poland syndrom
Polands sekvens
Polychondritis
Polycystisk nyresygdom, infantil
Polymyositis
Polyneuropathia inflammatorica acuta
Polyostotic fibrous dysplasia
Pompes sygdom
Pontocerebellar hypoplasi type 2
Porfyri
Porfyria cutanea tarda
Prader-Willi syndrom
Primær cilie dyskinesi
Primær hyperoxaluri type 1
Primær intrakraniel hypertension
Primær systemisk amyloidose
Progeria
Progressiv myoclonus epilepsi type 1
Progressiv partiel lipodystrofi
Progressive hemifacial atrophy
Prolaktinom
Prolaktinproducerende hypofyseadenom
Prolidase defekt
Propionic acidemia
Propionsyreæmi
Proteolipid protein
Proteus syndrom
Proximal femoral focal deficiency
Proximal fokal femurdefekt
Prune Belly syndrom
Prurigo Nodularis
Prurigo Nodularis Hyde
Pseudo-pseudohypoparathyreoidisme
Pseudohypoparathyreoidisme
Pseudotumor cerebri (”falsk hjernesvulst”)
Pseudoxanthoma elasticum
PXE
Pyknodysostose
Pyruvat dehydrogenase mangel
Pyruvat kinase defekt