Disease Directory

Atrial septal defect 7 is an extremely rare congenital heart condition that primarily affects the structure and electrical conduction of the heart. It...

Atrial septal defect 8 is a congenital heart condition characterized by an opening in the atrial septum resulting from a mutation in the CITED2 gene....

Atrial septal defect 9 is a congenital heart defect that affects the structure of the atrial septum, the wall that separates the heart’s upper chamber...

Atrial septal defect, coronary sinus type, is a specific form of atrial septal defect characterized by an abnormal opening between the heart's atria,...

Atrial septal defect, ostium primum type is a congenital heart defect characterized by an abnormal opening between the left and right atria resulting...

Atrial septal defect (ASD), ostium secundum type, is characterized by a defect in the atrial septum, leading to a left-to-right shunt. This condition...

Atrial septal defect, sinus venosus type, is a specific form of congenital heart defect characterized by an abnormal opening in the atrial septum, all...

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

Atrial standstill 1 is a cardiac conduction disorder characterized by the absence of normal electrical activity in the atria, which can lead to signif...

Atrial standstill 2 is a cardiac condition characterized by an absence of effective atrial contraction due to a mutation in the NPPA gene. This condit...

Atrichia with papular lesions is a rare inherited condition caused by variants in the HR gene, leading to irreversible hair loss during the neonatal p...

Atrioventricular defect-blepharophimosis-radial and anal defect syndrome is an extremely rare condition. Because few cases have been documented, detai...

Atrioventricular septal defect is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Atrioventricular septal defect 4 (AVSD4) is a congenital heart defect caused by mutations in the GATA4 gene. This condition is inherited in an autosom...

Atrioventricular septal defect 5 is a congenital heart condition marked by significant abnormalities in the structure of the heart. It is caused by mu...

Atrophic lichen planus is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Atrophic muscular disease, also known as atrophic muscular disorder, refers to a group of conditions marked by a reduction in muscle volume and atroph...

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

Atrophoderma of Pierini and Pasini is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

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