MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Acute endophthalmitis

ORPHA:279888Клин. подтип
Not applicable

Acute erythroid leukemia

ORPHA:318Заболевание
Not applicable

Acute fatty liver of pregnancy

ORPHA:243367Заболевание
Multigenic/multifactorial

Acute flaccid myelitis

ORPHA:623801Заболевание

Acute generalized exanthematous pustulosis

ORPHA:293173Заболевание
Multigenic/multifactorial, Not applicable

Acute hepatic porphyria

ORPHA:95157Клин. группа
Autosomal dominant, Autosomal recessive

Acute idiopathic maculopathy

ORPHA:714101Заболевание
Not applicable

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

ORPHA:217371Заболевание
Autosomal recessive

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

ORPHA:466794Заболевание
Autosomal recessive

Acute infantile liver failure-multisystemic involvement syndrome

ORPHA:370088Заболевание
Autosomal recessive

Acute inflammatory demyelinating polyradiculoneuropathy

ORPHA:98916Заболевание
Multigenic/multifactorial, Not applicable

Acute intermittent porphyria

ORPHA:79276Заболевание
Autosomal dominant

Acute interstitial pneumonia

ORPHA:79126Заболевание
Unknown

Acute leukemia of ambiguous lineage

ORPHA:86851Категория

Acute liver failure

ORPHA:90062Clinical syndrome
Not applicable

Acute lung injury

ORPHA:178320Особая клин. ситуация
Not applicable

Acute lymphoblastic leukemia

ORPHA:513Клин. группа

Acute macular neuroretinopathy

ORPHA:488239Заболевание

Acute mast cell leukemia

ORPHA:566393Клин. подтип
Not applicable

Acute megakaryoblastic leukemia

ORPHA:518Заболевание
Not applicable

Acute megakaryoblastic leukemia in children with Down syndrome

ORPHA:99887Клин. подтип
Not applicable

Acute megakaryoblastic leukemia in children without Down syndrome

ORPHA:329469Клин. подтип
Not applicable

Acute monoblastic/monocytic leukemia

ORPHA:514Заболевание
Not applicable

Acute motor and sensory axonal neuropathy

ORPHA:98917Заболевание
Multigenic/multifactorial, Not applicable