MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Inflammatory breast cancer

ORPHA:694963Заболевание

Inflammatory myofibroblastic tumor

ORPHA:178342Заболевание

Inflammatory myopathy with abundant macrophages

ORPHA:247718Заболевание
Not applicable

Inflammatory pseudotumor of the liver

ORPHA:90003Заболевание
Not applicable

Inhalational anthrax

ORPHA:247257Заболевание
Not applicable

Inhalational botulism

ORPHA:254504Клин. подтип

Inherited Creutzfeldt-Jakob disease

ORPHA:282166Заболевание
Autosomal dominant

Inherited acute myeloid leukemia

ORPHA:319465Заболевание
Autosomal dominant

Inherited arrhythmogenic cardiomyopathy

ORPHA:247Клин. группа
Autosomal dominant, Autosomal recessive

Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations

ORPHA:319462Заболевание
Autosomal recessive

Inherited congenital spastic tetraplegia

ORPHA:210141Заболевание
Autosomal recessive, Unknown

Inherited epidermodysplasia verruciformis

ORPHA:302Заболевание
Autosomal recessive

Inherited epidermolysis bullosa

ORPHA:79361Категория
Autosomal dominant, Autosomal recessive

Inherited ichthyosis

ORPHA:183435Категория

Inherited ichthyosis syndromic form

ORPHA:281085Категория

Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency

ORPHA:289548Заболевание
Autosomal recessive

Inherited isolated arrhythmogenic cardiomyopathy

ORPHA:217656Заболевание
Autosomal dominant

Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variant

ORPHA:293888Клин. подтип
Autosomal dominant

Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variant

ORPHA:293910Клин. подтип
Autosomal dominant

Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variant

ORPHA:293899Клин. подтип
Autosomal dominant

Inherited non-syndromic ichthyosis

ORPHA:281082Категория

Iniencephaly

ORPHA:63259Морф. аномалия
Multigenic/multifactorial, Not applicable

Insulin autoimmune syndrome

ORPHA:411593Заболевание
Not applicable

Insulin-resistance syndrome type A

ORPHA:2297Заболевание
Autosomal dominant, Autosomal recessive