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-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
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
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 paraplegia type 2
X-linked recessive
Childhood
Spastic paraplegia type 7
Autosomal dominant, Autosomal recessive
Adolescent, Adult, Childhood, Elderly
Spastic paraplegia-Paget disease of bone syndrome
Autosomal dominant
Adult
Spastic paraplegia-glaucoma-intellectual disability syndrome
Autosomal recessive
Adult
Spastic paraplegia-neuropathy-poikiloderma syndrome
Childhood
Spastic paraplegia-optic atrophy-neuropathy syndrome
Autosomal recessive
Childhood, Infancy