MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Thrombocytopenia with congenital dyserythropoietic anemia

ORPHA:67044Kr.
X-linked recessive

Thrombocytopenia-absent radius syndrome

ORPHA:3320Malf.
Autosomal recessive

Thrombomodulin-related bleeding disorder

ORPHA:436169Kr.
Autosomal dominant

Thrombotic thrombocytopenic purpura

ORPHA:54057Kr.
Autosomal recessive, Multigenic/multifactorial

Thumb deformity-alopecia-pigmentation anomaly syndrome

ORPHA:2251Malf.

Thumb stiffness-brachydactyly-intellectual disability syndrome

ORPHA:1078Malf.
Autosomal dominant

Thymic carcinoma

ORPHA:99868Kr.
Not applicable

Thymic epithelial neoplasm

ORPHA:3398Kat.
Autosomal recessive, Not applicable

Thymic neuroendocrine carcinoma

ORPHA:99869Kr.
Not applicable

Thymic neuroendocrine tumor

ORPHA:97289Kr.

Thymic-renal-anal-lung dysplasia

ORPHA:3326Malf.
Autosomal recessive

Thymoma

ORPHA:99867Kr.
Not applicable

Thymoma type A

ORPHA:263310His. subt.
Not applicable

Thymoma type AB

ORPHA:263324His. subt.
Not applicable

Thymoma type B

ORPHA:263317His. subt.
Not applicable

Thymoma-hypogammaglobulinemia syndrome

ORPHA:169105Kr.

Thyrocerebrorenal syndrome

ORPHA:3327Malf.
Autosomal recessive

Thyroid ectopia

ORPHA:95712Morph.
Not applicable

Thyroid hemiagenesis

ORPHA:95719Morph.
Not applicable

Thyroid hypoplasia

ORPHA:95720Morph.
Autosomal dominant, Not applicable

Thyroid lymphoma

ORPHA:97285Kr.

Thyrotoxic periodic paralysis

ORPHA:79102Kr.
Multigenic/multifactorial, Not applicable

Tibial aplasia-ectrodactyly syndrome

ORPHA:3329Malf.
Autosomal dominant

Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome

ORPHA:988Malf.
Autosomal dominant, Autosomal recessive