Peroxisome biogenesis disorder

Autosomal recessive

Infancy, Neonatal

Perrault syndrome

Autosomal recessive

Adolescent, Adult, Childhood

Perrault syndrome type 1

Perrault syndrome type 2

Perry syndrome

Autosomal dominant

Adult

Persistent Müllerian duct syndrome

Autosomal recessive

Infancy

Persistent hyperplastic primary vitreous

Autosomal dominant, Autosomal recessive

Infancy, Neonatal

Persistent idiopathic facial pain

Adult

Persistent placoid maculopathy

Adult, Elderly

Persistent polyclonal B-cell lymphocytosis

Multigenic/multifactorial

No data available

Peters anomaly

Autosomal dominant, Autosomal recessive

Infancy, Neonatal

Peters plus syndrome

Autosomal recessive

Antenatal, Neonatal

Peutz-Jeghers syndrome

Autosomal dominant

Adolescent, Adult, Childhood

Pfeiffer syndrome

Autosomal dominant

Antenatal, Neonatal

Pfeiffer syndrome type 1

Autosomal dominant, Not applicable

Antenatal, Neonatal

Pfeiffer syndrome type 2

Autosomal dominant, Not applicable

Antenatal, Neonatal

Pfeiffer syndrome type 3

Autosomal dominant, Not applicable

Antenatal, Neonatal

Pfeiffer-Palm-Teller syndrome

Neonatal

Phacoanaphylactic uveitis

Not applicable

Adult

Phakomatosis cesioflammea

Not applicable

Phakomatosis cesiomarmorata

Not applicable

Phakomatosis pigmentokeratotica

Unknown

Infancy, Neonatal

Phakomatosis pigmentovascularis

Not applicable

Neonatal

Phakomatosis spilorosea

Not applicable