MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Pulmonary valve agenesis

ORPHA:982Clin. grp.
Not applicable

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

ORPHA:101206Malform.

Pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis

ORPHA:431353Cat.

Pulmonary venoocclusive disease

ORPHA:31837Disease
Autosomal recessive, Not applicable

Pulverulent cataract

ORPHA:98984Clin. sub.
Autosomal dominant, Autosomal recessive

Punctate acrokeratoderma freckle-like pigmentation

ORPHA:99710Disease

Punctate inner choroidopathy

ORPHA:580951Disease

Punctate palmoplantar keratoderma type 1

ORPHA:79501Disease
Autosomal dominant

Punctate palmoplantar keratoderma type 2

ORPHA:79502Disease
Autosomal dominant

Pure autonomic failure

ORPHA:441Disease
Not applicable

Pure hair and nail ectodermal dysplasia

ORPHA:69084Malform.
Autosomal dominant, Autosomal recessive

Pure mitochondrial myopathy

ORPHA:254854Disease
Mitochondrial inheritance

Pure or complex autosomal dominant spastic paraplegia

ORPHA:320342Clin. grp.
Autosomal dominant

Pure or complex autosomal recessive spastic paraplegia

ORPHA:320346Clin. grp.
Autosomal recessive

Pure squamous carcinoma of the urothelial tract

ORPHA:695023Disease
Not applicable

Purine nucleoside phosphorylase deficiency

ORPHA:760Disease
Autosomal recessive

Pustular pyoderma gangrenosum

ORPHA:538866Clin. sub.
Multigenic/multifactorial

Pustulosis palmaris et plantaris

ORPHA:163927Disease
Autosomal dominant, Autosomal recessive

Pycnodysostosis

ORPHA:763Disease
Autosomal recessive

Pyknoachondrogenesis

ORPHA:3003Malform.
Autosomal recessive

Pyle disease

ORPHA:3005Disease
Autosomal recessive

Pyoderma gangrenosum

ORPHA:48104Disease
Unknown

Pyomyositis

ORPHA:764Disease
Not applicable

Pyramidal molars-abnormal upper lip syndrome

ORPHA:2561Malform.
Autosomal recessive