Aorto-ventricular tunnel is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Information about overview is currently limited for this condition.

Apert syndrome is a congenital craniofacial malformation disorder that is classified as a type of acrocephalosyndactyly, characterized primarily by cr...

Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome is an extremely rare congenital malformation syndrome characterized by underdevelopm...

Aphalangy-syndactyly-microcephaly syndrome is an extremely rare malformation syndrome characterized by partial distal aphalangia, syndactyly, duplicat...

Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome is an extremely rare condition. Because few cases have been documen...

Aplasia cutis autosomal recessive is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Aplasia cutis congenita dominant is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Aplasia cutis congenita-intestinal lymphangiectasia syndrome is an extremely rare condition characterized by congenital absence of skin on the head an...

Aplasia cutis-myopia syndrome is a rare genetic disorder characterized by the combination of aplasia cutis congenita, high myopia, congenital nystagmu...

Aplasia of the lacrimal and salivary glands (ALSG) is a rare disorder that primarily affects the development of the tear and saliva-producing glands....

Aplastic anemia is a disorder of the blood system that results from bone marrow failure, leading to markedly decreased production of red blood cells w...

Apnea of prematurity is a developmental disorder that affects premature infants by causing pauses in breathing often accompanied by a reduced heart ra...

APO A-i deficiency is a condition that has been recognized in clinical settings but remains not fully characterized in terms of its presentation and u...

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

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

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

Information about the overview is currently limited for this condition.

Apolipoprotein C-III deficiency is associated with variants in the APOC3 gene, which plays a crucial role in lipid metabolism. While the exact inherit...

Apparent mineralocorticoid excess (AME) is an endocrine and renal disorder that causes the body to behave as though it is producing too much of the sa...