MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

T-cell prolymphocytic leukemia

ORPHA:86871Заболевание
Not applicable

T-cell/histiocyte rich large B cell lymphoma

ORPHA:300857Заболевание
Multigenic/multifactorial, Not applicable

TAFRO syndrome

ORPHA:457077Заболевание
Not applicable

TARDBP-related predominantly upper-limb distal myopathy

ORPHA:700154Заболевание
Autosomal dominant

TARP syndrome

ORPHA:2886Мальформация
X-linked recessive

TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome

ORPHA:488632Мальформация
Autosomal recessive

TCR-alpha-beta-positive T-cell deficiency

ORPHA:397959Заболевание
Autosomal recessive

TELO2-related intellectual disability-neurodevelopmental disorder

ORPHA:488642Мальформация
Autosomal recessive

TEMPI syndrome

ORPHA:284227Clinical syndrome

TFR2-related hemochromatosis

ORPHA:225123Заболевание
Autosomal recessive

THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome

ORPHA:363444Мальформация
Autosomal recessive

TLR8-related inflammation-severe neutropenia-bone marrow failure-lymphoproliferation syndrome

ORPHA:675628Заболевание
X-linked recessive

TMEM165-CDG

ORPHA:314667Заболевание
Autosomal recessive

TMEM199-CDG

ORPHA:466703Заболевание
Autosomal recessive

TMEM70-related mitochondrial encephalo-cardio-myopathy

ORPHA:1194Заболевание
Autosomal recessive

TMEM94-associated congenital heart defect-facial dysmorphism-developmental delay syndrome

ORPHA:562569Мальформация
Autosomal recessive

TNP03-related limb-girdle muscular dystrophy D2

ORPHA:55595Заболевание
Autosomal dominant

TOR1AIP1-related limb-girdle muscular dystrophy

ORPHA:424261Заболевание
Autosomal recessive

TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome

ORPHA:592570Мальформация
Autosomal dominant

TRAPPC11-related limb-girdle muscular dystrophy R18

ORPHA:369840Заболевание
Autosomal recessive

TRIM22-related inflammatory bowel disease

ORPHA:597201Заболевание
Autosomal recessive

TRIM32-related limb-girdle muscular dystrophy R8

ORPHA:1878Заболевание
Autosomal recessive

TSH-secreting pituitary adenoma

ORPHA:91347Заболевание

Takayasu arteritis

ORPHA:3287Заболевание
Not applicable