Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Small cell lung cancer
Not applicable
Adult
Smith-Lemli-Opitz syndrome
Autosomal recessive
Antenatal, Infancy, Neonatal
Smith-Magenis syndrome
Autosomal dominant
Adolescent, Adult, Childhood, Infancy, Neonatal
Smith-McCort dysplasia
Autosomal recessive
Childhood
Smoldering systemic mastocytosis
Autosomal dominant, Unknown
Adult, Elderly
Snakebite envenomation
Not applicable
All ages
Sneddon syndrome
Autosomal dominant, Not applicable
Adult
Snowflake vitreoretinal degeneration
Autosomal dominant
Adult
Soft tissue sarcoma
Solar urticaria
Not applicable
All ages
Solitary bone cyst
Not applicable
Childhood
Solitary fibrous tumor
Not applicable
All ages
Solitary rectal ulcer syndrome
Not applicable
Adult
Somatomammotropinoma
Adolescent, Adult
Somatostatinoma
Unknown
Adult, Elderly
Sorsby fundus dystrophy
Autosomal dominant
Adult
Sotos syndrome
Autosomal dominant, Autosomal recessive
Antenatal, Neonatal
Southeast Asian ovalocytosis
Autosomal dominant
All ages
Spasmus nutans
Unknown
Infancy
Spastic ataxia with congenital miosis
Autosomal dominant
Adolescent, Childhood, Infancy, Neonatal
Spastic ataxia-corneal dystrophy syndrome
Autosomal recessive
Childhood
Spastic ataxia-dysarthria due to glutaminase deficiency
Autosomal dominant
Childhood
Spastic paraparesis-cataracts-speech delay syndrome
Autosomal dominant
Spastic paraparesis-deafness syndrome
Childhood