MEDLIB
Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер
Табылды 3,968 заболеваний (Ауру) Қалпына келтіру

Actinic lichen planus

ORPHA:254395Ауру

Actinic prurigo

ORPHA:330061Ауру
Multigenic/multifactorial, Not applicable

Actinomycosis

ORPHA:457095Ауру
Not applicable

Actinomyopathy-associated syndromic thrombocytopenia

ORPHA:674653Ауру
Autosomal dominant

Action myoclonus-renal failure syndrome

ORPHA:163696Ауру
Autosomal recessive

Activated PI3K-delta syndrome 1

ORPHA:693661Ауру
Autosomal dominant

Activated PI3K-delta syndrome 2

ORPHA:693681Ауру
Autosomal dominant

Acute ackee fruit intoxication

ORPHA:73423Ауру
Not applicable

Acute annular outer retinopathy

ORPHA:284460Ауру
Not applicable

Acute basophilic leukemia

ORPHA:86849Ауру

Acute disseminated encephalomyelitis

ORPHA:83597Ауру
Not applicable

Acute encephalopathy with biphasic seizures and late reduced diffusion

ORPHA:363549Ауру

Acute erythroid leukemia

ORPHA:318Ауру
Not applicable

Acute fatty liver of pregnancy

ORPHA:243367Ауру
Multigenic/multifactorial

Acute flaccid myelitis

ORPHA:623801Ауру

Acute generalized exanthematous pustulosis

ORPHA:293173Ауру
Multigenic/multifactorial, Not applicable

Acute idiopathic maculopathy

ORPHA:714101Ауру
Not applicable

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

ORPHA:217371Ауру
Autosomal recessive

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

ORPHA:466794Ауру
Autosomal recessive

Acute infantile liver failure-multisystemic involvement syndrome

ORPHA:370088Ауру
Autosomal recessive

Acute inflammatory demyelinating polyradiculoneuropathy

ORPHA:98916Ауру
Multigenic/multifactorial, Not applicable

Acute intermittent porphyria

ORPHA:79276Ауру
Autosomal dominant

Acute interstitial pneumonia

ORPHA:79126Ауру
Unknown

Acute macular neuroretinopathy

ORPHA:488239Ауру