Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Polyarteritis nodosa
Not applicable
All ages
Polycythemia vera
Not applicable
All ages
Polyembryoma
Not applicable
Adolescent, Adult
Polyendocrine-polyneuropathy syndrome
Autosomal recessive
Childhood
Polyglucosan body myopathy type 1
Autosomal recessive
Adolescent, Childhood
Polyglucosan body myopathy type 2
Autosomal recessive
Adolescent, Adult, Childhood, Elderly
Polyhydramnios-megalencephaly-symptomatic epilepsy syndrome
Autosomal recessive
Antenatal, Infancy, Neonatal
Polymerase proofreading-related polyposis
Autosomal dominant
Childhood
Polymyositis
Not applicable
Adult, Elderly
Polyneuropathy associated with IgM monoclonal gammopathy
Not applicable
Adult, Elderly
Polyneuropathy-hearing loss-ataxia-retinitis pigmentosa-cataract syndrome
Autosomal recessive
Childhood
Pontiac fever
Not applicable
All ages
Pontine autosomal dominant microangiopathy with leukoencephalopathy
Autosomal dominant
Adult
Porencephaly
Multigenic/multifactorial, Not applicable
Antenatal, Infancy, Neonatal
Porokeratosis of Mibelli
Autosomal dominant, Not applicable
Adolescent, Adult, Childhood
Porokeratosis plantaris palmaris et disseminata
Autosomal dominant, X-linked dominant
Adolescent, Adult
Porokeratotic eccrine ostial and dermal duct nevus
Not applicable
Infancy, Neonatal
Porphyria cutanea tarda
Autosomal dominant, Multigenic/multifactorial
Adult
Porphyria due to ALA dehydratase deficiency
Autosomal recessive
Adolescent, Childhood
Portosinusoidal vascular disease
Adult
Post 5-alpha-reductase inhibitors treatment syndrome
Not applicable
Post-selective serotonin reuptake inhibitor sexual dysfunction
Not applicable
Post-transplant lymphoproliferative disease
Not applicable
All ages
Post-traumatic pituitary deficiency
Adolescent, Adult, Childhood, Elderly