MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Transcobalamin deficiency

ORPHA:859Kr.
Autosomal recessive

Transgrediens et progrediens palmoplantar keratoderma

ORPHA:495Kr.

Transient erythroblastopenia of childhood

ORPHA:98871Kr.

Transient familial neonatal hyperbilirubinemia

ORPHA:2312Kr.

Transient hyperammonemia of the newborn

ORPHA:289877spez. Sit.

Transient infantile hypertriglyceridemia and hepatosteatosis

ORPHA:300293Kr.
Autosomal recessive

Transient myeloproliferative syndrome

ORPHA:420611Kr.
Not applicable

Transient neonatal diabetes mellitus

ORPHA:99886Kr.
Autosomal dominant, Autosomal recessive, Not applicable

Transient neonatal multiple acyl-CoA dehydrogenase deficiency

ORPHA:329942Kr.
Autosomal dominant

Transient neonatal myasthenia gravis

ORPHA:391504Kl. subt.
Not applicable

Transient predisposition to invasive pyogenic bacterial infection

ORPHA:70592Kr.
Autosomal recessive

Transient pseudohypoaldosteronism

ORPHA:93164Kr.
Not applicable

Transient tyrosinemia of the newborn

ORPHA:3402Kr.

Transitional cell carcinoma of the corpus uteri

ORPHA:213746Kr.

Transketolase deficiency

ORPHA:488618Malf.
Autosomal recessive

Transposition of the great arteries

ORPHA:216675Kat.
Multigenic/multifactorial, Not applicable

Treacher-Collins syndrome

ORPHA:861Malf.
Autosomal dominant, Autosomal recessive

Trehalase deficiency

ORPHA:103909Kr.
Autosomal dominant

Tremor-ataxia-central hypomyelination syndrome

ORPHA:447896Kl. subt.
Autosomal recessive

Tremor-nystagmus-duodenal ulcer syndrome

ORPHA:3350Kr.

Trench fever

ORPHA:64694Kr.

Trichinellosis

ORPHA:863Kr.
Not applicable

Tricho-dento-osseous syndrome

ORPHA:3352Malf.
Autosomal dominant

Tricho-retino-dento-digital syndrome

ORPHA:1264Malf.
Autosomal dominant