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

Polyarteritis nodosa

ORPHA:767Kr.
Not applicable

Polycythemia vera

ORPHA:729Kr.
Not applicable

Polyembryoma

ORPHA:180229Kr.
Not applicable

Polyendocrine-polyneuropathy syndrome

ORPHA:453533Kr.
Autosomal recessive

Polyglucosan body myopathy type 1

ORPHA:397937Kr.
Autosomal recessive

Polyglucosan body myopathy type 2

ORPHA:456369Kr.
Autosomal recessive

Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome

ORPHA:500533Kr.
Autosomal recessive

Polymerase proofreading-related polyposis

ORPHA:447877Kr.
Autosomal dominant

Polymyositis

ORPHA:732Kr.
Not applicable

Polyneuropathy associated with IgM monoclonal gammopathy

ORPHA:209004Kr.
Not applicable

Polyneuropathy-hearing loss-ataxia-retinitis pigmentosa-cataract syndrome

ORPHA:171848Kr.
Autosomal recessive

Pontiac fever

ORPHA:99748Kr.
Not applicable

Pontine autosomal dominant microangiopathy with leukoencephalopathy

ORPHA:477749Kr.
Autosomal dominant

Porencephaly

ORPHA:2940Kr.
Multigenic/multifactorial, Not applicable

Porokeratosis of Mibelli

ORPHA:735Kr.
Autosomal dominant, Not applicable

Porokeratosis plantaris palmaris et disseminata

ORPHA:737Kr.
Autosomal dominant, X-linked dominant

Porokeratotic eccrine ostial and dermal duct nevus

ORPHA:166286Kr.
Not applicable

Porphyria cutanea tarda

ORPHA:101330Kr.
Autosomal dominant, Multigenic/multifactorial

Porphyria due to ALA dehydratase deficiency

ORPHA:100924Kr.
Autosomal recessive

Portosinusoidal vascular disease

ORPHA:596937Kr.

Post 5-alpha-reductase inhibitors treatment syndrome

ORPHA:686468Kr.
Not applicable

Post-selective serotonin reuptake inhibitor sexual dysfunction

ORPHA:686475Kr.
Not applicable

Post-transplant lymphoproliferative disease

ORPHA:70568Kr.
Not applicable

Post-traumatic pituitary deficiency

ORPHA:95619Kr.