MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Synpolydactyly type 2

ORPHA:295197Kl. subt.
Autosomal dominant

Syringocystadenoma papilliferum

ORPHA:840Kr.
Unknown

Syringomyelia

ORPHA:3280Kl. gruppe
Not applicable

Systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood

ORPHA:364033Kr.
Not applicable

Systemic capillary leak syndrome

ORPHA:188Kr.
Not applicable

Systemic diseases with anterior uveitis

ORPHA:280926Kat.

Systemic lupus erythematosus

ORPHA:536Kr.
Not applicable

Systemic mastocytosis

ORPHA:2467Kl. gruppe
Not applicable

Systemic mastocytosis with associated hematologic neoplasm

ORPHA:98849Kr.
Not applicable

Systemic monochloroacetate poisoning

ORPHA:90069Kr.

Systemic polyarteritis nodosa

ORPHA:439762Kl. subt.
Not applicable

Systemic primary carnitine deficiency

ORPHA:158Kr.
Autosomal recessive

Systemic sclerosis

ORPHA:90291Kr.
Multigenic/multifactorial, Not applicable

Systemic-onset juvenile idiopathic arthritis

ORPHA:85414Kr.
Multigenic/multifactorial, Unknown

Sézary syndrome

ORPHA:3162Kr.
Multigenic/multifactorial, Not applicable

T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta

ORPHA:169160Kr.
Autosomal recessive

T-B+ severe combined immunodeficiency due to CD45 deficiency

ORPHA:169157Kr.
Autosomal recessive

T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency

ORPHA:169154Kr.
Autosomal recessive

T-B+ severe combined immunodeficiency due to JAK3 deficiency

ORPHA:35078Kr.
Autosomal recessive

T-B+ severe combined immunodeficiency due to gamma chain deficiency

ORPHA:276Kr.
X-linked recessive

T-cell immunodeficiency with epidermodysplasia verruciformis

ORPHA:324294Kr.
Autosomal recessive

T-cell immunodeficiency with thymic aplasia

ORPHA:83471Kr.
Autosomal recessive

T-cell large granular lymphocyte leukemia

ORPHA:86872Kr.
Not applicable

T-cell non-Hodgkin lymphoma

ORPHA:171918Kat.