MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Postencephalitic parkinsonism

ORPHA:97349Kr.

Posterior amorphous corneal dystrophy

ORPHA:98971Kr.
Autosomal dominant

Posterior column ataxia-retinitis pigmentosa syndrome

ORPHA:88628Kr.
Autosomal recessive

Posterior cortical atrophy

ORPHA:54247Kr.
Unknown

Posterior polymorphous corneal dystrophy

ORPHA:98973Kr.
Autosomal dominant

Postinfectious cerebellitis

ORPHA:624244Kr.

Postinfectious vasculitis

ORPHA:48435Kr.
Not applicable

Postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome

ORPHA:477673Kr.
Autosomal recessive

Postpartum psychosis

ORPHA:443173Kr.
Not applicable

Postpoliomyelitis syndrome

ORPHA:2942Kr.
Not applicable

Postural orthostatic tachycardia syndrome due to NET deficiency

ORPHA:443236Kr.
Autosomal dominant

PrP systemic amyloidosis

ORPHA:397606Kr.
Autosomal dominant

Prader-Willi syndrome

ORPHA:739Kr.
Autosomal dominant, Not applicable

Pre-Descemet corneal dystrophy

ORPHA:293462Kr.
Unknown

Precursor B-cell acute lymphoblastic leukemia

ORPHA:99860Kr.
Not applicable

Precursor T-cell acute lymphoblastic leukemia

ORPHA:99861Kr.
Not applicable

Predisposition to invasive fungal disease due to CARD9 deficiency

ORPHA:457088Kr.
Autosomal recessive

Predisposition to severe viral infection due to IRF7 deficiency

ORPHA:574918Kr.
Autosomal recessive

Preeclampsia

ORPHA:275555Kr.
Not applicable

Prenatal-onset spinal muscular atrophy with congenital bone fractures

ORPHA:486811Kr.
Autosomal recessive

Pressure-induced localized lipoatrophy

ORPHA:90160Kr.

Presumed ocular histoplasmosis syndrome

ORPHA:714160Kr.
Not applicable

Primary CD59 deficiency

ORPHA:169464Kr.
Autosomal recessive

Primary Fanconi renotubular syndrome

ORPHA:3337Kr.
Autosomal dominant, Autosomal recessive