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База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы
Найдено 3,968 заболеваний (Disease) Сброс

Polyarteritis nodosa

ORPHA:767Disease
Not applicable

Polycythemia vera

ORPHA:729Disease
Not applicable

Polyembryoma

ORPHA:180229Disease
Not applicable

Polyendocrine-polyneuropathy syndrome

ORPHA:453533Disease
Autosomal recessive

Polyglucosan body myopathy type 1

ORPHA:397937Disease
Autosomal recessive

Polyglucosan body myopathy type 2

ORPHA:456369Disease
Autosomal recessive

Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome

ORPHA:500533Disease
Autosomal recessive

Polymerase proofreading-related polyposis

ORPHA:447877Disease
Autosomal dominant

Polymyositis

ORPHA:732Disease
Not applicable

Polyneuropathy associated with IgM monoclonal gammopathy

ORPHA:209004Disease
Not applicable

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

ORPHA:171848Disease
Autosomal recessive

Pontiac fever

ORPHA:99748Disease
Not applicable

Pontine autosomal dominant microangiopathy with leukoencephalopathy

ORPHA:477749Disease
Autosomal dominant

Porencephaly

ORPHA:2940Disease
Multigenic/multifactorial, Not applicable

Porokeratosis of Mibelli

ORPHA:735Disease
Autosomal dominant, Not applicable

Porokeratosis plantaris palmaris et disseminata

ORPHA:737Disease
Autosomal dominant, X-linked dominant

Porokeratotic eccrine ostial and dermal duct nevus

ORPHA:166286Disease
Not applicable

Porphyria cutanea tarda

ORPHA:101330Disease
Autosomal dominant, Multigenic/multifactorial

Porphyria due to ALA dehydratase deficiency

ORPHA:100924Disease
Autosomal recessive

Portosinusoidal vascular disease

ORPHA:596937Disease

Post 5-alpha-reductase inhibitors treatment syndrome

ORPHA:686468Disease
Not applicable

Post-selective serotonin reuptake inhibitor sexual dysfunction

ORPHA:686475Disease
Not applicable

Post-transplant lymphoproliferative disease

ORPHA:70568Disease
Not applicable

Post-traumatic pituitary deficiency

ORPHA:95619Disease