Disease Directory

Amelogenesis imperfecta type 1G is an extremely rare condition that primarily affects dental enamel formation and kidney tissue, leading to hypoplasti...

Amelogenesis imperfecta type 1H is a condition affecting the development of dental enamel, leading to abnormalities in the appearance and structure of...

Amelogenesis imperfecta type 2 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Amelogenesis imperfecta type 2A1 is an inherited dental condition characterized by abnormal enamel formation. This disorder is caused by mutations in...

Amelogenesis imperfecta type 3B (AI3B) is a genetic condition characterized by enamel hypomineralization, leading to defects in the enamel structure....

Amelogenesis imperfecta, IIa 1K, is a genetic condition characterized by defects in enamel formation. It is caused by variants in the SP6 gene and fol...

Amelogenesis imperfecta, hypomaturation type, IIa6 is a genetic condition caused by variants in the GPR68 gene. It is inherited in an autosomal recess...

Amelogenesis imperfecta, type 1J is a genetic condition associated with variants in the ACP4 gene, which plays a role in enamel formation. This condit...

Amelogenesis imperfecta, type 3A is a hereditary dental condition affecting the formation and quality of tooth enamel. This condition is caused by pat...

Amelogenesis imperfecta, type 3C (AI3C) is a genetic condition caused by variants in the RELT gene, which is inherited in an autosomal recessive manne...

Ameloonychohypohidrotic syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Aminoacylase 1 deficiency is an inherited metabolic condition that primarily affects the brain and other body systems. It results from pathogenic vari...

Aminopterin/methotrexate embryofetopathy is an extremely rare condition. Because few cases have been documented, detailed clinical information is limi...

Amniotic band syndrome is a group of sporadic congenital anomalies that occur in association with fibrous amniotic bands, affecting the limbs, craniof...

Information about the overall nature of amniotic fluid embolism is currently limited for this condition. At times, the condition is noted in trusted r...

Amoebiasis due to Entamoeba histolytica is an infection caused by a parasitic protozoa that primarily affects the gastrointestinal system. The disease...

Amoebiasis due to free-living amoebae is an infection primarily affecting the central nervous system, with the potential to cause devastating conditio...

Ampulla of vater adenocarcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Ampulla of vater adenosquamous carcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limi...

Ampulla of vater cancer is a malignant neoplasm involving the ampulla of Vater, a critical anatomical area where the bile and pancreatic ducts converg...