Orphanet Database • Orphadata CC-BY-4.0
Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
7,547
Заболеваний
4 552
Генов
8 700
Фенотипов
140
Регионов
Все (7,547)Biological anomalyCategoryClinical groupClinical subtypeClinical syndromeDiseaseEtiological subtypeHistopathological subtypeMalformation syndromeMorphological anomalyParticular clinical situation in a disease or syndrome
Parana hard skin syndrome
Infancy
Paraneoplastic cerebellar degeneration
All ages
Paraneoplastic isolated brainstem encephalitis
All ages
Paraneoplastic neurologic syndrome
Not applicable
All ages
Paraneoplastic pemphigus
Not applicable
All ages
Paraneoplastic uveitis
Adult
Paraparetic variant of Guillain-Barré syndrome
Multigenic/multifactorial, Not applicable
All ages
Paraplegia-intellectual disability-hyperkeratosis syndrome
X-linked recessive
Infancy
Paraquat poisoning
Not applicable
All ages
Parasitic myositis
All ages
Paraspinal arteriovenous malformation
Not applicable
Paratesticular adenocarcinoma
Adult
Parathyroid carcinoma
Not applicable
Adult
Paratyphoid fever
Not applicable
All ages
Parenteral nutrition-associated cholestasis
All ages
Parietal encephalocele
Parietal foramina with clavicular hypoplasia
Autosomal dominant
Infancy, Neonatal
Paris-Trousseau thrombocytopenia
Infancy, Neonatal
Parkes Weber syndrome
Autosomal dominant, Not applicable
Infancy, Neonatal
Parkinson-dementia complex of Guam
Parkinsonian-pyramidal syndrome
Autosomal recessive
Adolescent, Adult
Parkinsonism with polyneuropathy
Adult
Paroxysmal cold hemoglobinuria
Multigenic/multifactorial
Childhood
Paroxysmal dyskinesia
Autosomal dominant, Not applicable
Childhood