Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Primary cutaneous T-cell lymphoma
Primary cutaneous amyloidosis
Autosomal dominant, Not applicable
All ages
Primary cutaneous anaplastic large cell lymphoma
Adolescent, Adult, Childhood
Primary cutaneous lymphoma
Primary cutaneous peripheral T-cell lymphoma not otherwise specified
Not applicable
Adult, Elderly
Primary cutaneous plasmacytosis
Not applicable
Adult, Elderly
Primary cutis verticis gyrata
All ages
Primary dystonia, DYT13 type
Autosomal dominant
Adolescent, Childhood
Primary dystonia, DYT17 type
Autosomal recessive
Adolescent, Adult
Primary dystonia, DYT2 type
Autosomal recessive
Childhood
Primary dystonia, DYT21 type
Autosomal dominant
Adult
Primary dystonia, DYT27 type
Autosomal recessive
Adult, Childhood
Primary dystonia, DYT4 type
Autosomal dominant
Adolescent, Adult
Primary dystonia, DYT6 type
Autosomal dominant
Adolescent, Adult, Childhood
Primary effusion lymphoma
Adult
Primary erythromelalgia
Autosomal dominant
All ages
Primary essential cutis verticis gyrata
Adolescent, Adult
Primary failure of tooth eruption
Autosomal dominant
Primary familial polycythemia
Autosomal dominant
All ages
Primary hepatic neuroendocrine carcinoma
Not applicable
Adult
Primary hyperaldosteronism-seizures-neurological abnormalities syndrome
Not applicable
Infancy, Neonatal
Primary hypereosinophilic syndrome
All ages
Primary hypergonadotropic hypogonadism-partial alopecia syndrome
Autosomal recessive
Neonatal
Primary hyperoxaluria
Autosomal recessive
All ages