Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Inflammatory breast cancer
Inflammatory myofibroblastic tumor
Inflammatory myopathy with abundant macrophages
Not applicable
Inflammatory pseudotumor of the liver
Not applicable
All ages
Inhalational anthrax
Not applicable
All ages
Inhalational botulism
Adult
Inherited Creutzfeldt-Jakob disease
Autosomal dominant
Adult, Elderly
Inherited acute myeloid leukemia
Autosomal dominant
Inherited arrhythmogenic cardiomyopathy
Autosomal dominant, Autosomal recessive
Adolescent, Adult
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
Autosomal recessive
Inherited congenital spastic tetraplegia
Autosomal recessive, Unknown
Infancy, Neonatal
Inherited epidermodysplasia verruciformis
Autosomal recessive
All ages
Inherited epidermolysis bullosa
Autosomal dominant, Autosomal recessive
All ages
Inherited ichthyosis
Inherited ichthyosis syndromic form
Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency
Autosomal recessive
Infancy, Neonatal
Inherited isolated arrhythmogenic cardiomyopathy
Autosomal dominant
No data available
Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variant
Autosomal dominant
Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variant
Autosomal dominant
Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variant
Autosomal dominant
Inherited non-syndromic ichthyosis
Iniencephaly
Multigenic/multifactorial, Not applicable
Infancy, Neonatal
Insulin autoimmune syndrome
Not applicable
Adult, Elderly
Insulin-resistance syndrome type A
Autosomal dominant, Autosomal recessive
Adolescent, Adult, Childhood