MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

T-cell prolymphocytic leukemia

ORPHA:86871Kr.
Not applicable

T-cell/histiocyte rich large B cell lymphoma

ORPHA:300857Kr.
Multigenic/multifactorial, Not applicable

TAFRO syndrome

ORPHA:457077Kr.
Not applicable

TARDBP-related predominantly upper-limb distal myopathy

ORPHA:700154Kr.
Autosomal dominant

TARP syndrome

ORPHA:2886Malf.
X-linked recessive

TBCK-related encephalopathy-severe hypotonia-craniofacial dysmorphism syndrome

ORPHA:488632Malf.
Autosomal recessive

TCR-alpha-beta-positive T-cell deficiency

ORPHA:397959Kr.
Autosomal recessive

TELO2-related intellectual disability-neurodevelopmental disorder

ORPHA:488642Malf.
Autosomal recessive

TEMPI syndrome

ORPHA:284227Clinical syndrome

TFR2-related hemochromatosis

ORPHA:225123Kr.
Autosomal recessive

THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome

ORPHA:363444Malf.
Autosomal recessive

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

ORPHA:675628Kr.
X-linked recessive

TMEM165-CDG

ORPHA:314667Kr.
Autosomal recessive

TMEM199-CDG

ORPHA:466703Kr.
Autosomal recessive

TMEM70-related mitochondrial encephalo-cardio-myopathy

ORPHA:1194Kr.
Autosomal recessive

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

ORPHA:562569Malf.
Autosomal recessive

TNP03-related limb-girdle muscular dystrophy D2

ORPHA:55595Kr.
Autosomal dominant

TOR1AIP1-related limb-girdle muscular dystrophy

ORPHA:424261Kr.
Autosomal recessive

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

ORPHA:592570Malf.
Autosomal dominant

TRAPPC11-related limb-girdle muscular dystrophy R18

ORPHA:369840Kr.
Autosomal recessive

TRIM22-related inflammatory bowel disease

ORPHA:597201Kr.
Autosomal recessive

TRIM32-related limb-girdle muscular dystrophy R8

ORPHA:1878Kr.
Autosomal recessive

TSH-secreting pituitary adenoma

ORPHA:91347Kr.

Takayasu arteritis

ORPHA:3287Kr.
Not applicable