Disease Directory

Ichthyosis, congenital, autosomal recessive 12 is a form of congenital ichthyosis that primarily affects the skin, leading to abnormal scaling and imp...

Ichthyosis, lamellar, autosomal dominant is a congenital skin condition characterized by abnormal skin scaling and thickening. Research has identified...

Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome is a multisystem condition primarily affecting the skin, liver, spleen, and cerebellum....

Ichthyosis-oral and digital anomalies syndrome is a very rare condition characterized by distinctive skin findings, facial features, and digital anoma...

Idiopathic CD4 lymphocytopenia is a rare primary immunodeficiency disorder characterized by persistently low levels of CD4 T-cells, often defined as l...

Idiopathic CD4-positive T-lymphocytopenia is a rare immunodeficiency syndrome that is defined by a decrease in CD4-positive lymphocytes to below 300 p...

Idiopathic acute eosinophilic pneumonia is a lung condition characterized by the sudden onset of fever, severe shortness of breath, and hypoxic respir...

Idiopathic acute transverse myelitis is an immune-mediated inflammatory disorder that affects the spinal cord, leading to motor, sensory, and autonomi...

Idiopathic anterior uveitis is an inflammatory condition affecting the front part of the eye, particularly the anterior uveal tract. The term ‘idiopat...

Idiopathic aplastic anemia is a disorder of the blood in which the bone marrow fails to produce sufficient blood cells, resulting in a range of hemato...

Idiopathic bronchiectasis (IB) is a progressive lung condition marked by chronic dilation and destruction of the bronchial walls without any clearly i...