MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Actinic lichen planus

ORPHA:254395Kr.

Actinic prurigo

ORPHA:330061Kr.
Multigenic/multifactorial, Not applicable

Actinomycosis

ORPHA:457095Kr.
Not applicable

Actinomyopathy-associated syndromic thrombocytopenia

ORPHA:674653Kr.
Autosomal dominant

Action myoclonus-renal failure syndrome

ORPHA:163696Kr.
Autosomal recessive

Activated PI3K-delta syndrome 1

ORPHA:693661Kr.
Autosomal dominant

Activated PI3K-delta syndrome 2

ORPHA:693681Kr.
Autosomal dominant

Acute ackee fruit intoxication

ORPHA:73423Kr.
Not applicable

Acute annular outer retinopathy

ORPHA:284460Kr.
Not applicable

Acute basophilic leukemia

ORPHA:86849Kr.

Acute disseminated encephalomyelitis

ORPHA:83597Kr.
Not applicable

Acute encephalopathy with biphasic seizures and late reduced diffusion

ORPHA:363549Kr.

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 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 macular neuroretinopathy

ORPHA:488239Kr.