MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Small cell lung cancer

ORPHA:70573Заболевание
Not applicable

Smith-Lemli-Opitz syndrome

ORPHA:818Мальформация
Autosomal recessive

Smith-Magenis syndrome

ORPHA:819Мальформация
Autosomal dominant

Smith-McCort dysplasia

ORPHA:178355Заболевание
Autosomal recessive

Smoldering systemic mastocytosis

ORPHA:158775Заболевание
Autosomal dominant, Unknown

Snakebite envenomation

ORPHA:449285Заболевание
Not applicable

Sneddon syndrome

ORPHA:820Заболевание
Autosomal dominant, Not applicable

Snowflake vitreoretinal degeneration

ORPHA:91496Заболевание
Autosomal dominant

Soft tissue sarcoma

ORPHA:3394Клин. группа

Solar urticaria

ORPHA:97230Заболевание
Not applicable

Solitary bone cyst

ORPHA:83468Заболевание
Not applicable

Solitary fibrous tumor

ORPHA:2126Заболевание
Not applicable

Solitary rectal ulcer syndrome

ORPHA:209964Заболевание
Not applicable

Somatomammotropinoma

ORPHA:314769Заболевание

Somatostatinoma

ORPHA:97283Заболевание
Unknown

Sorsby fundus dystrophy

ORPHA:59181Заболевание
Autosomal dominant

Sotos syndrome

ORPHA:821Заболевание
Autosomal dominant, Autosomal recessive

Southeast Asian ovalocytosis

ORPHA:98868Заболевание
Autosomal dominant

Spasmus nutans

ORPHA:279882Clinical syndrome
Unknown

Spastic ataxia with congenital miosis

ORPHA:1182Заболевание
Autosomal dominant

Spastic ataxia-corneal dystrophy syndrome

ORPHA:2572Заболевание
Autosomal recessive

Spastic ataxia-dysarthria due to glutaminase deficiency

ORPHA:557056Заболевание
Autosomal dominant

Spastic paraparesis-cataracts-speech delay syndrome

ORPHA:615938Clinical syndrome
Autosomal dominant

Spastic paraparesis-deafness syndrome

ORPHA:2815Мальформация