MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Pulmonary valve agenesis

ORPHA:982Kl. gruppe
Not applicable

Pulmonary valve agenesis-tetralogy of Fallot-absence of ductus arteriosus syndrome

ORPHA:101206Malf.

Pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis

ORPHA:431353Kat.

Pulmonary venoocclusive disease

ORPHA:31837Kr.
Autosomal recessive, Not applicable

Pulverulent cataract

ORPHA:98984Kl. subt.
Autosomal dominant, Autosomal recessive

Punctate acrokeratoderma freckle-like pigmentation

ORPHA:99710Kr.

Punctate inner choroidopathy

ORPHA:580951Kr.

Punctate palmoplantar keratoderma type 1

ORPHA:79501Kr.
Autosomal dominant

Punctate palmoplantar keratoderma type 2

ORPHA:79502Kr.
Autosomal dominant

Pure autonomic failure

ORPHA:441Kr.
Not applicable

Pure hair and nail ectodermal dysplasia

ORPHA:69084Malf.
Autosomal dominant, Autosomal recessive

Pure mitochondrial myopathy

ORPHA:254854Kr.
Mitochondrial inheritance

Pure or complex autosomal dominant spastic paraplegia

ORPHA:320342Kl. gruppe
Autosomal dominant

Pure or complex autosomal recessive spastic paraplegia

ORPHA:320346Kl. gruppe
Autosomal recessive

Pure squamous carcinoma of the urothelial tract

ORPHA:695023Kr.
Not applicable

Purine nucleoside phosphorylase deficiency

ORPHA:760Kr.
Autosomal recessive

Pustular pyoderma gangrenosum

ORPHA:538866Kl. subt.
Multigenic/multifactorial

Pustulosis palmaris et plantaris

ORPHA:163927Kr.
Autosomal dominant, Autosomal recessive

Pycnodysostosis

ORPHA:763Kr.
Autosomal recessive

Pyknoachondrogenesis

ORPHA:3003Malf.
Autosomal recessive

Pyle disease

ORPHA:3005Kr.
Autosomal recessive

Pyoderma gangrenosum

ORPHA:48104Kr.
Unknown

Pyomyositis

ORPHA:764Kr.
Not applicable

Pyramidal molars-abnormal upper lip syndrome

ORPHA:2561Malf.
Autosomal recessive