MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Inflammatory breast cancer

ORPHA:694963Kr.

Inflammatory myofibroblastic tumor

ORPHA:178342Kr.

Inflammatory myopathy with abundant macrophages

ORPHA:247718Kr.
Not applicable

Inflammatory pseudotumor of the liver

ORPHA:90003Kr.
Not applicable

Inhalational anthrax

ORPHA:247257Kr.
Not applicable

Inhalational botulism

ORPHA:254504Kl. subt.

Inherited Creutzfeldt-Jakob disease

ORPHA:282166Kr.
Autosomal dominant

Inherited acute myeloid leukemia

ORPHA:319465Kr.
Autosomal dominant

Inherited arrhythmogenic cardiomyopathy

ORPHA:247Kl. gruppe
Autosomal dominant, Autosomal recessive

Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations

ORPHA:319462Kr.
Autosomal recessive

Inherited congenital spastic tetraplegia

ORPHA:210141Kr.
Autosomal recessive, Unknown

Inherited epidermodysplasia verruciformis

ORPHA:302Kr.
Autosomal recessive

Inherited epidermolysis bullosa

ORPHA:79361Kat.
Autosomal dominant, Autosomal recessive

Inherited ichthyosis

ORPHA:183435Kat.

Inherited ichthyosis syndromic form

ORPHA:281085Kat.

Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency

ORPHA:289548Kr.
Autosomal recessive

Inherited isolated arrhythmogenic cardiomyopathy

ORPHA:217656Kr.
Autosomal dominant

Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variant

ORPHA:293888Kl. subt.
Autosomal dominant

Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variant

ORPHA:293910Kl. subt.
Autosomal dominant

Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variant

ORPHA:293899Kl. subt.
Autosomal dominant

Inherited non-syndromic ichthyosis

ORPHA:281082Kat.

Iniencephaly

ORPHA:63259Morph.
Multigenic/multifactorial, Not applicable

Insulin autoimmune syndrome

ORPHA:411593Kr.
Not applicable

Insulin-resistance syndrome type A

ORPHA:2297Kr.
Autosomal dominant, Autosomal recessive