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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Acute endophthalmitis

ORPHA:279888Clin. sub.
Not applicable

Acute erythroid leukemia

ORPHA:318Disease
Not applicable

Acute fatty liver of pregnancy

ORPHA:243367Disease
Multigenic/multifactorial

Acute flaccid myelitis

ORPHA:623801Disease

Acute generalized exanthematous pustulosis

ORPHA:293173Disease
Multigenic/multifactorial, Not applicable

Acute hepatic porphyria

ORPHA:95157Clin. grp.
Autosomal dominant, Autosomal recessive

Acute idiopathic maculopathy

ORPHA:714101Disease
Not applicable

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

ORPHA:217371Disease
Autosomal recessive

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

ORPHA:466794Disease
Autosomal recessive

Acute infantile liver failure-multisystemic involvement syndrome

ORPHA:370088Disease
Autosomal recessive

Acute inflammatory demyelinating polyradiculoneuropathy

ORPHA:98916Disease
Multigenic/multifactorial, Not applicable

Acute intermittent porphyria

ORPHA:79276Disease
Autosomal dominant

Acute interstitial pneumonia

ORPHA:79126Disease
Unknown

Acute leukemia of ambiguous lineage

ORPHA:86851Cat.

Acute liver failure

ORPHA:90062Clinical syndrome
Not applicable

Acute lung injury

ORPHA:178320Situation
Not applicable

Acute lymphoblastic leukemia

ORPHA:513Clin. grp.

Acute macular neuroretinopathy

ORPHA:488239Disease

Acute mast cell leukemia

ORPHA:566393Clin. sub.
Not applicable

Acute megakaryoblastic leukemia

ORPHA:518Disease
Not applicable

Acute megakaryoblastic leukemia in children with Down syndrome

ORPHA:99887Clin. sub.
Not applicable

Acute megakaryoblastic leukemia in children without Down syndrome

ORPHA:329469Clin. sub.
Not applicable

Acute monoblastic/monocytic leukemia

ORPHA:514Disease
Not applicable

Acute motor and sensory axonal neuropathy

ORPHA:98917Disease
Multigenic/multifactorial, Not applicable