Disease Directory

Hinman syndrome, also known as non-neurogenic neurogenic bladder or Hinman-Allen syndrome, is a condition affecting how the bladder empties. It is con...

Hirschsprung disease (HSCR) is a congenital disorder that affects the large intestine. It occurs when a part of the colon is missing the nerve cells n...

Hirschsprung disease-ganglioneuroblastoma syndrome is a rare genetic disorder that occurs due to a developmental defect during embryogenesis. It is ch...

Hirschsprung disease-hearing loss-polydactyly syndrome is an extremely rare condition that has been described in only two siblings. It is characterize...

Hirschsprung disease-nail hypoplasia-dysmorphism syndrome is a rare and severe disorder that affects many parts of the body. The condition is characte...

Hirschsprung disease-type D brachydactyly syndrome is a rare condition that is defined by the presence of Hirschsprung disease and a specific hand and...

His bundle tachycardia is a very rare congenital genetic condition affecting the heart's rhythm. It is characterized by a persistent rapid heartbeat t...

Histoplasma capsulatum infectious disease is a condition caused by an infection with the fungus Histoplasma capsulatum. This disease is also known by...

Histoplasma pericarditis is a condition characterized by inflammation of the pericardium due to infection with the Histoplasma fungus. While specific...

Hodgkin's lymphoma, lymphocytic depletion is a diffuse subtype of classical Hodgkin lymphoma characterized by an abundance of Hodgkin and Reed-Sternbe...

Hodgkin's lymphoma, lymphocytic-histiocytic predominance is a subtype of classical Hodgkin lymphoma characterized by the presence of scattered Hodgkin...

Hodgkin's lymphoma, mixed cellularity is a subtype of classical Hodgkin lymphoma characterized by the presence of scattered Reed-Sternberg and Hodgkin...

Hodgkin lymphoma, also known as HL or Hodgkin disease, is a type of cancer that mainly affects the lymph nodes. It is a group of malignant lymphoid ne...

Hogue-Janssens syndrome 1 is an autosomal dominant intellectual developmental disorder. It is caused by a mutation in the PPP2R5D gene, which plays a...

Holmes-Adie syndrome is a rare condition that is mainly known for an unusually dilated pupil and reduced reflexes. It is also associated with abnormal...

Holt-Oram syndrome is a rare genetic condition known as the most common form of heart-hand syndrome. It is named for its combined impact on the heart...

Holzgreve-Wagner-Rehder syndrome is a rare condition characterized by a series of congenital abnormalities. People with this condition can have featur...

Hordnes Engebretsen Knudtson syndrome is a rare disease. Detailed information about this condition is currently limited in medical literature.

Horner syndrome is a rare condition that affects the nerves of the face. It is known for causing three main signs: a smaller (constricted) pupil (mios...

Information about overview is currently limited for this condition.