Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Short stature-delayed bone age due to thyroid hormone metabolism deficiency
Autosomal recessive
Childhood, Infancy
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome
Autosomal recessive
Infancy, Neonatal
Short stature-pituitary and cerebellar defects-small sella turcica syndrome
Autosomal dominant
Infancy, Neonatal
Short-limb skeletal dysplasia with severe combined immunodeficiency
Not applicable
Infancy, Neonatal
Shwachman-Diamond syndrome
Autosomal recessive
Antenatal, Childhood, Infancy, Neonatal
Sialidosis type 1
Autosomal recessive
Adolescent, Childhood
Sialidosis type 2
Autosomal recessive
Antenatal, Childhood, Infancy, Neonatal
Sialuria
Autosomal dominant
Infancy
Sickle cell S-C disease
Autosomal recessive
All ages
Sickle cell anemia
Autosomal recessive
All ages
Sickle cell-beta-thalassemia disease
Autosomal recessive
All ages
Silent sinus syndrome
Not applicable
Adult
Silver-Russell syndrome
Autosomal dominant, Not applicable
Antenatal, Neonatal
Simple cryoglobulinemia
Adult, Elderly
Sinding-Larsen-Johansson disease
Not applicable
Adolescent, Childhood
Sinoatrial node dysfunction and deafness
Autosomal recessive
Infancy, Neonatal
Sitosterolemia
Autosomal recessive
All ages
Sjögren-Larsson syndrome
Autosomal recessive
Infancy, Neonatal
Skeletal Ewing sarcoma
Not applicable
All ages
Skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome
Autosomal recessive
Antenatal, Neonatal
Skin fragility-woolly hair-palmoplantar keratoderma syndrome
Autosomal dominant, Autosomal recessive
Childhood
Sleep-related hypermotor epilepsy
Autosomal dominant
Adolescent, Adult, Childhood
Small cell carcinoma of the bladder
Not applicable
Adult
Small cell carcinoma of the ovary
Not applicable
Adolescent, Adult, Childhood, Infancy