| D059446 |
Heterotaxy Syndrome |
Abnormal thoracoabdominal VISCERA arrangement (visceral heterotaxy) or malformation that involves additional CONGENITAL HEART DEFECTS (e.g., heart isomerism; DEXTROCARDIA) and/or abnormal SPLEEN (e.g., asplenia and polysplenia). Irregularities with the central nervous system, the skeleton and urinary tract are often associated with the syndrome. |
Asplenia Syndrome,Asplenia with Cardiovascular Anomalies,Ivemark Syndrome,Left Atrial Isomerism,Left Atrial Isomerism with Polysplenia,Polysplenia Syndrome,Right Atrial Isomerism,Right Atrial Isomerism with Asplenia,Situs Ambiguus,Situs Ambiguus Viscerum,Situs Ambiguus with Asplenia,Situs Ambiguus with Polysplenia,Visceral Heterotaxy,Ambiguus Viscerum, Situs,Ambiguus Viscerums, Situs,Ambiguus, Situs,Asplenia Syndromes,Atrial Isomerism, Left,Atrial Isomerism, Right,Atrial Isomerisms, Left,Atrial Isomerisms, Right,Heterotaxies, Visceral,Heterotaxy Syndromes,Heterotaxy, Visceral,Isomerism, Left Atrial,Isomerism, Right Atrial,Isomerisms, Left Atrial,Isomerisms, Right Atrial,Left Atrial Isomerisms,Polysplenia Syndromes,Right Atrial Isomerisms,Situs Ambiguus Viscerums,Syndrome, Asplenia,Syndrome, Heterotaxy,Syndrome, Ivemark,Syndrome, Polysplenia,Syndromes, Asplenia,Syndromes, Heterotaxy,Syndromes, Polysplenia,Visceral Heterotaxies,Viscerum, Situs Ambiguus,Viscerums, Situs Ambiguus |
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| D040181 |
Genetic Diseases, X-Linked |
Genetic diseases that are linked to gene mutations on the X CHROMOSOME in humans (X CHROMOSOME, HUMAN) or the X CHROMOSOME in other species. Included here are animal models of human X-linked diseases. |
X-Linked Genetic Diseases,Genetic Diseases, X-Chromosome Linked,Disease, X-Linked Genetic,Diseases, X-Linked Genetic,Genetic Disease, X-Linked,Genetic Diseases, X Chromosome Linked,Genetic Diseases, X Linked,X Linked Genetic Diseases,X-Linked Genetic Disease |
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