Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Paratyphoid fever
Not applicable
All ages
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 dystonic choreathetosis with episodic ataxia and spasticity
Autosomal dominant
Childhood
Paroxysmal exertion-induced dyskinesia
Autosomal dominant, Not applicable
Adolescent, Adult, Childhood, Infancy
Paroxysmal extreme pain disorder
Autosomal dominant
Infancy, Neonatal
Paroxysmal hemicrania
Not applicable
Adolescent, Adult, Childhood, Elderly
Paroxysmal kinesigenic dyskinesia
Autosomal dominant, Not applicable
Adolescent, Adult, Childhood, Infancy
Paroxysmal nocturnal hemoglobinuria
Not applicable
All ages
Paroxysmal non-kinesigenic dyskinesia
Autosomal dominant, Not applicable
Adolescent, Adult, Childhood, Infancy
Partial androgen insensitivity syndrome
X-linked recessive
All ages
Partially involuting congenital hemangioma
Not applicable
Antenatal
Pauci-immune glomerulonephritis
Not applicable
Adolescent, Adult, Childhood, Elderly
Pearson syndrome
Mitochondrial inheritance, Not applicable
Childhood, Infancy, Neonatal
Pediatric acute respiratory distress syndrome
Pediatric collagenous gastritis
Adolescent, Childhood, Infancy
Pediatric hepatocellular carcinoma
Not applicable
Adolescent, Childhood
Pediatric multiple sclerosis
Adolescent, Childhood
Pediatric systemic lupus erythematosus
Not applicable
Adolescent, Childhood, Infancy, Neonatal
Pediatric-onset Graves disease
Adolescent, Childhood, Infancy