MEDLIB
База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы

Tularemia

ORPHA:3392Заболевание
Not applicable

Tumor necrosis factor receptor 1 associated periodic syndrome

ORPHA:32960Заболевание
Autosomal dominant

Tumor of cranial and spinal nerves

ORPHA:252057Кат.

Tumor of endocrine glands

ORPHA:182130Кат.

Tumor of testis and paratestis

ORPHA:363472Кат.

Tungiasis

ORPHA:879Заболевание
Not applicable

Turner syndrome

ORPHA:881Порок
Not applicable, Unknown

Turner syndrome due to structural X chromosome anomalies

ORPHA:99413Этиол. подт.

Turnpenny-Fry syndrome

ORPHA:688642Порок
Autosomal dominant

Twin anemia-polycythemia sequence

ORPHA:617294Заболевание

Twin-reversed arterial perfusion sequence

ORPHA:617297Заболевание

Typhoid

ORPHA:99745Заболевание
Not applicable

Typical nemaline myopathy

ORPHA:171436Заболевание
Autosomal dominant, Autosomal recessive

Typical urticaria pigmentosa

ORPHA:158766Клин. подт.
Autosomal dominant, Unknown

Tyrosinemia type 1

ORPHA:882Заболевание
Autosomal recessive

Tyrosinemia type 2

ORPHA:28378Заболевание
Autosomal recessive

Tyrosinemia type 3

ORPHA:69723Заболевание
Autosomal recessive

UMOD-related autosomal dominant tubulointerstitial kidney disease

ORPHA:88950Клин. подт.
Autosomal dominant

UV-sensitive syndrome

ORPHA:178338Заболевание
Autosomal recessive

Uhl anomaly

ORPHA:3403Морф.
Not applicable

Ulbright-Hodes syndrome

ORPHA:3404Порок
Autosomal recessive

Ulerythema ophryogenesis

ORPHA:3406Заболевание
Autosomal dominant, Not applicable

Ullrich congenital muscular dystrophy

ORPHA:75840Заболевание
Autosomal dominant, Autosomal recessive

Ulna hypoplasia-intellectual disability syndrome

ORPHA:2249Порок
Autosomal recessive