MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen

B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality

ORPHA:585877Ätl. subt.

B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1)

ORPHA:585929Ätl. subt.

B-lymphoblastic leukemia/lymphoma with t(17;19)

ORPHA:641375Ätl. subt.

B-lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3)

ORPHA:585956Ätl. subt.

B-lymphoblastic leukemia/lymphoma with t(5;14)(q31.1;q32.3)

ORPHA:585948Ätl. subt.

B-lymphoblastic leukemia/lymphoma with t(7;9)(q11.2;p13.2)

ORPHA:641372Ätl. subt.

B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)

ORPHA:585909Ätl. subt.
Not applicable

B-lymphoblastic leukemia/lymphoma with t(v;11q23.3)

ORPHA:585918Ätl. subt.

B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome

ORPHA:536467Kl. subt.
Autosomal recessive

B4GALT1-CDG

ORPHA:79332Kr.
Autosomal recessive

B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome

ORPHA:75496Kl. subt.
Autosomal recessive

BAG3-related myofibrillar myopathy

ORPHA:199340Kr.
Autosomal dominant

BAP1-related tumor predisposition syndrome

ORPHA:289539Kr.
Autosomal dominant

BENTA disease

ORPHA:464336Kr.
Autosomal dominant

BICD2-related autosomal dominant childhood-onset proximal spinal muscular atrophy

ORPHA:363454Ätl. subt.
Autosomal dominant

BNAR syndrome

ORPHA:217266Malf.
Autosomal recessive

BOR syndrome

ORPHA:107Malf.
Autosomal dominant

BPTF-related intellectual disability-facial dysmorphism-skeletal anomalies syndrome

ORPHA:686482Malf.
Autosomal dominant

BRESEK syndrome

ORPHA:85284Malf.
X-linked dominant

BVES-related limb-girdle muscular dystrophy

ORPHA:476084Kr.
Autosomal recessive

Babesiosis

ORPHA:108Kr.
Not applicable

Bacterial myositis

ORPHA:206994Kr.

Bacterial toxic-shock syndrome

ORPHA:36234Kr.
Not applicable

Bainbridge-Ropers syndrome

ORPHA:352577Kr.
Autosomal dominant, Not applicable