MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
3,968 diseases matched (Disease) Reset

Idiopathic macular telangiectasia type 1

ORPHA:353344Disease

Idiopathic macular telangiectasia type 3

ORPHA:353351Disease

Idiopathic neonatal atrial flutter

ORPHA:45452Disease
Not applicable

Idiopathic panuveitis

ORPHA:280921Disease
Not applicable

Idiopathic peliosis hepatis

ORPHA:480524Disease

Idiopathic phalangeal acro-osteolysis

ORPHA:444316Disease
Not applicable

Idiopathic pleuroparenchymal fibroelastosis

ORPHA:494428Disease

Idiopathic pulmonary fibrosis

ORPHA:2032Disease
Multigenic/multifactorial

Idiopathic pulmonary hemosiderosis

ORPHA:99931Disease

Idiopathic recurrent pericarditis

ORPHA:251307Disease
Not applicable

Idiopathic recurrent stupor

ORPHA:276174Disease
Not applicable

Idiopathic spontaneous coronary artery dissection

ORPHA:458718Disease
Not applicable

Idiopathic trachyonychia

ORPHA:79153Disease
Autosomal dominant

Idiopathic uveal effusion syndrome

ORPHA:209956Disease
Unknown

Idiopathic ventricular fibrillation

ORPHA:228140Disease
Autosomal dominant, Not applicable

Idiopathic/heritable pulmonary arterial hypertension

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

IgA pemphigus

ORPHA:555905Disease

IgG4-related systemic disease

ORPHA:596448Disease
Not applicable

Ileal neuroendocrine tumor

ORPHA:100078Disease
Not applicable

Imerslund-Gräsbeck syndrome

ORPHA:35858Disease
Autosomal recessive

Iminoglycinuria

ORPHA:42062Disease
Autosomal recessive

Immune dysregulation with immunodeficiency due to AIOLOS haploinsufficiency

ORPHA:699590Disease
Autosomal recessive

Immune dysregulation-inflammatory bowel disease- recurrent sinopulmonary infections syndrome

ORPHA:529980Disease

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

ORPHA:238569Disease
Autosomal recessive