Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Actinic lichen planus
All ages
Actinic prurigo
Multigenic/multifactorial, Not applicable
Childhood
Actinomycosis
Not applicable
All ages
Actinomyopathy-associated syndromic thrombocytopenia
Autosomal dominant
Action myoclonus-renal failure syndrome
Autosomal recessive
Adolescent, Adult
Activated PI3K-delta syndrome 1
Autosomal dominant
Activated PI3K-delta syndrome 2
Autosomal dominant
Acute ackee fruit intoxication
Not applicable
All ages
Acute annular outer retinopathy
Not applicable
Adult
Acute basophilic leukemia
All ages
Acute disseminated encephalomyelitis
Not applicable
All ages
Acute encephalopathy with biphasic seizures and late reduced diffusion
Infancy, Neonatal
Acute erythroid leukemia
Not applicable
Adolescent, Adult, Childhood, Elderly
Acute fatty liver of pregnancy
Multigenic/multifactorial
Adult
Acute flaccid myelitis
Adolescent, Adult, Childhood, Infancy
Acute generalized exanthematous pustulosis
Multigenic/multifactorial, Not applicable
All ages
Acute idiopathic maculopathy
Not applicable
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Autosomal recessive
Infancy, Neonatal
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome
Autosomal recessive
Infancy
Acute infantile liver failure-multisystemic involvement syndrome
Autosomal recessive
Infancy, Neonatal
Acute inflammatory demyelinating polyradiculoneuropathy
Multigenic/multifactorial, Not applicable
All ages
Acute intermittent porphyria
Autosomal dominant
Adolescent, Adult
Acute interstitial pneumonia
Unknown
Adult
Acute macular neuroretinopathy
Adolescent, Adult