MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen

Acute endophthalmitis

ORPHA:279888Kl. subt.
Not applicable

Acute erythroid leukemia

ORPHA:318Kr.
Not applicable

Acute fatty liver of pregnancy

ORPHA:243367Kr.
Multigenic/multifactorial

Acute flaccid myelitis

ORPHA:623801Kr.

Acute generalized exanthematous pustulosis

ORPHA:293173Kr.
Multigenic/multifactorial, Not applicable

Acute hepatic porphyria

ORPHA:95157Kl. gruppe
Autosomal dominant, Autosomal recessive

Acute idiopathic maculopathy

ORPHA:714101Kr.
Not applicable

Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins

ORPHA:217371Kr.
Autosomal recessive

Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome

ORPHA:466794Kr.
Autosomal recessive

Acute infantile liver failure-multisystemic involvement syndrome

ORPHA:370088Kr.
Autosomal recessive

Acute inflammatory demyelinating polyradiculoneuropathy

ORPHA:98916Kr.
Multigenic/multifactorial, Not applicable

Acute intermittent porphyria

ORPHA:79276Kr.
Autosomal dominant

Acute interstitial pneumonia

ORPHA:79126Kr.
Unknown

Acute leukemia of ambiguous lineage

ORPHA:86851Kat.

Acute liver failure

ORPHA:90062Clinical syndrome
Not applicable

Acute lung injury

ORPHA:178320spez. Sit.
Not applicable

Acute lymphoblastic leukemia

ORPHA:513Kl. gruppe

Acute macular neuroretinopathy

ORPHA:488239Kr.

Acute mast cell leukemia

ORPHA:566393Kl. subt.
Not applicable

Acute megakaryoblastic leukemia

ORPHA:518Kr.
Not applicable

Acute megakaryoblastic leukemia in children with Down syndrome

ORPHA:99887Kl. subt.
Not applicable

Acute megakaryoblastic leukemia in children without Down syndrome

ORPHA:329469Kl. subt.
Not applicable

Acute monoblastic/monocytic leukemia

ORPHA:514Kr.
Not applicable

Acute motor and sensory axonal neuropathy

ORPHA:98917Kr.
Multigenic/multifactorial, Not applicable