MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Ulnar hypoplasia-split foot syndrome

ORPHA:1122Мальформация

Ulnar-mammary syndrome

ORPHA:3138Мальформация
Autosomal dominant

Ulnar/fibula ray defect-brachydactyly syndrome

ORPHA:52056Мальформация
Autosomal dominant

Umbilical cord ulceration-intestinal atresia syndrome

ORPHA:3405Мальформация
Unknown

Unclassified acute myeloid leukemia

ORPHA:167714Категория

Unclassified autoinflammatory syndrome

ORPHA:324936Категория

Unclassified myelodysplastic syndrome

ORPHA:98827Заболевание
Not applicable

Unclassified vasculitis

ORPHA:251328Заболевание
Not applicable

Uncombable hair syndrome

ORPHA:1410Заболевание
Autosomal recessive

Undifferentiated carcinoma of esophagus

ORPHA:418951Заболевание
Not applicable

Undifferentiated carcinoma of liver and intrahepatic biliary tract

ORPHA:424970Заболевание
Not applicable

Undifferentiated carcinoma of stomach

ORPHA:423786Заболевание
Not applicable

Undifferentiated carcinoma with osteoclast-like giant cells of pancreas

ORPHA:424080Заболевание
Not applicable

Undifferentiated pleomorphic sarcoma

ORPHA:2023Заболевание
Not applicable

Unexplained long-lasting fever/inflammatory syndrome

ORPHA:251332Заболевание

Unicentric Castleman disease

ORPHA:93685Клин. подтип

Unifocal Langerhans cell histiocytosis

ORPHA:687730Клин. подтип
Not applicable

Unilateral focal polymicrogyria

ORPHA:268947Клин. подтип

Unilateral hemispheric polymicrogyria

ORPHA:101071Клин. подтип

Unilateral multicystic dysplastic kidney

ORPHA:97363Клин. подтип
Autosomal dominant

Unilateral ocular duplication

ORPHA:3374Морф. аномалия
Autosomal dominant

Unilateral polymicrogyria

ORPHA:268943Морф. аномалия

Univentricular heart

ORPHA:1464Морф. аномалия
Not applicable

Unspecified juvenile idiopathic arthritis

ORPHA:91140Заболевание