MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов
Найдено 3,968 заболеваний (Заболевание)Сбросить

Idiopathic macular telangiectasia type 1

ORPHA:353344Заболевание

Idiopathic macular telangiectasia type 3

ORPHA:353351Заболевание

Idiopathic neonatal atrial flutter

ORPHA:45452Заболевание
Not applicable

Idiopathic panuveitis

ORPHA:280921Заболевание
Not applicable

Idiopathic peliosis hepatis

ORPHA:480524Заболевание

Idiopathic phalangeal acro-osteolysis

ORPHA:444316Заболевание
Not applicable

Idiopathic pleuroparenchymal fibroelastosis

ORPHA:494428Заболевание

Idiopathic pulmonary fibrosis

ORPHA:2032Заболевание
Multigenic/multifactorial

Idiopathic pulmonary hemosiderosis

ORPHA:99931Заболевание

Idiopathic recurrent pericarditis

ORPHA:251307Заболевание
Not applicable

Idiopathic recurrent stupor

ORPHA:276174Заболевание
Not applicable

Idiopathic spontaneous coronary artery dissection

ORPHA:458718Заболевание
Not applicable

Idiopathic trachyonychia

ORPHA:79153Заболевание
Autosomal dominant

Idiopathic uveal effusion syndrome

ORPHA:209956Заболевание
Unknown

Idiopathic ventricular fibrillation

ORPHA:228140Заболевание
Autosomal dominant, Not applicable

Idiopathic/heritable pulmonary arterial hypertension

ORPHA:422Заболевание
Autosomal dominant, Autosomal recessive, Not applicable

IgA pemphigus

ORPHA:555905Заболевание

IgG4-related systemic disease

ORPHA:596448Заболевание
Not applicable

Ileal neuroendocrine tumor

ORPHA:100078Заболевание
Not applicable

Imerslund-Gräsbeck syndrome

ORPHA:35858Заболевание
Autosomal recessive

Iminoglycinuria

ORPHA:42062Заболевание
Autosomal recessive

Immune dysregulation with immunodeficiency due to AIOLOS haploinsufficiency

ORPHA:699590Заболевание
Autosomal recessive

Immune dysregulation-inflammatory bowel disease- recurrent sinopulmonary infections syndrome

ORPHA:529980Заболевание

Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome

ORPHA:238569Заболевание
Autosomal recessive