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
Seborrhea-like dermatitis with psoriasiform elements
Autosomal dominant
Childhood
Seckel syndrome
Autosomal recessive
Antenatal
Secondary erythromelalgia
All ages
Secondary hypereosinophilic syndrome
All ages
Secondary hypoparathyroidism due to impaired parathormon secretion
Not applicable
Adolescent, Adult, Childhood, Elderly
Secondary intestinal lymphangiectasia
Adult, Elderly
Secondary neonatal autoimmune disease
Neonatal
Secondary non-traumatic avascular necrosis
Not applicable
Adult
Secondary polyarteritis nodosa
Not applicable
Secondary polycythemia
Autosomal dominant, Autosomal recessive
All ages
Secondary pulmonary alveolar proteinosis
Not applicable
Secondary sclerosing cholangitis
Not applicable
Secondary short bowel syndrome
Not applicable
All ages
Secondary syringomyelia
Adult
Segmental odontomaxillary dysplasia
Not applicable
Childhood
Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome
Not applicable
Neonatal
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Not applicable
Antenatal, Neonatal
Segmental venous malformation
Not applicable
Childhood, Neonatal
Seizures-intellectual disability due to hydroxylysinuria syndrome
Autosomal recessive
Infancy
Seizures-scoliosis-macrocephaly syndrome
Autosomal recessive
Infancy
Selective IgM deficiency
All ages
Selective intrauterine growth restriction
Antenatal
Self-healing papular mucinosis
All ages
Self-improving collodion baby
Autosomal recessive
Neonatal