Disease Directory

Hereditary cerebellar ataxia is a condition primarily affecting the cerebellum, the part of the brain responsible for coordination and balance. It run...

Hereditary chronic pancreatitis is an inherited form of pancreatitis characterized by recurrent episodes of acute inflammation that over time lead to...

Hereditary clear cell renal cell carcinoma is an inherited form of kidney cancer that presents as a malignant epithelial neoplasm, most commonly in th...

Hereditary coproporphyria is a form of acute hepatic porphyria that primarily disrupts heme synthesis and manifests through neuro-visceral attacks, wi...

Hereditary cryohydrocytosis with reduced stomatin is a very rare multisystem condition that affects blood, the central nervous system, and other organ...

Hereditary dementia is an inherited form of dementia characterized by progressive cognitive decline resulting from a genomic modification. Variants in...

Hereditary diffuse gastric adenocarcinoma is a form of stomach cancer that originates in the lining of the stomach and is characterized by the presenc...

Hereditary disease refers to a group of conditions caused by genetic modifications that are passed from parent to child. This condition arises from va...

Hereditary elliptocytosis is a rare disorder affecting the red blood cell membrane, and it is characterized by abnormal cell shapes that can lead to h...

Hereditary endocrine growth disease is a disorder that affects the regulation of growth through the endocrine system. Although detailed information ab...

Hereditary epidermal appendage anomaly is a genetic condition that affects the skin’s structures, which include components such as hair, nails, and sw...

Hereditary folate malabsorption is an inherited disorder affecting the transport of folate, leading to a systemic and central nervous system deficienc...

Hereditary gastric cancer describes a familial tendency to develop cancer of the stomach, often evident when two or more affected relatives are observ...