Phenotypes for disease #02238 (HTX1 (heterotaxy, visceral, X-linked, type 1, (HTX-1, situs inversus/situs ambiguus)), OMIM:306955)

36 entries on 1 page. Showing entries 1 - 36.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000025071 heterotaxy with complex cardiac malformations - - Familial, X-linked recessive - - - - - Patrice Bouvagnet 00029040
0000045646 Heterotaxy, gut malrotation, asplenia, ASD, CAVC, PA - - Familial, X-linked recessive - - - - - Aimee Paulussen 00059056
0000045647 ASD, VSD, DORV, PS, TGA, cholestatic liver disease, imperforate anus, bilat club feet, fused lumbar vertebrae. - - Familial - - - - - Aimee Paulussen 00059057
0000045648 AVSD, DORV, PAPVR, malrotation, transverse liver, asplenia. - - Unknown - - - - - Aimee Paulussen 00059058
0000045649 d-TGA, PDA - - Isolated (sporadic) - - - - - Aimee Paulussen 00059059
0000045650 Heterotaxy, Midline liver, dextrocardia, CAVC, PA, DORV, TAPVR. - - Isolated (sporadic) - - - - - Aimee Paulussen 00059060
0000045651 Heterotaxy, dextrocardia, VSD, ventriculomegaly, no stomach. - - Isolated (sporadic) - - - - - Aimee Paulussen 00059061
0000045652 Two male fetuses with heterotaxy, one living male with heterotaxy and caudal regression syndrome - - Familial, X-linked recessive - - - - - Aimee Paulussen 00059062
0000045653 Three male fetuses with heterotaxy syndrome. - - Familial, X-linked recessive - - - - - Aimee Paulussen 00059063
0000045654 Two male fetuses with heterotaxy syndrome. - - Unknown - - - - - Aimee Paulussen 00059064
0000045655 Male fetus with complex CHD (DORV, TGA, AVSD) and isomerism. - - Familial, X-linked recessive - - - - - Aimee Paulussen 00059065
0000045656 Asymptomatic, familial history of male heterotaxy (2 brothers died of heterotaxy) - - Familial, X-linked recessive - - - - - Aimee Paulussen 00059066
0000045657 Two male fetuses with heterotaxy syndrome. - - Familial, X-linked recessive - - - - - Aimee Paulussen 00059067
0000045661 Female with AVSD, pulmonary atresia and TAPVR, also abdominal malrotation. - - Familial - - - - - Aimee Paulussen 00059071
0000045662 Congenital heart disease. - - Isolated (sporadic) - - - - - Aimee Paulussen 00059072
0000045663 TGA - - Familial - - - - - Aimee Paulussen 00059073
0000045664 PA, VSD, ASD. - - Isolated (sporadic) - - - - - Aimee Paulussen 00059074
0000045665 Asymptomatic, familial history of male dextrocardia and heterotaxy. - - Familial - - - - - Aimee Paulussen 00059075
0000045666 Two male deaths with heterotaxy - - Familial, X-linked recessive - - - - - Aimee Paulussen 00059076
0000045667 Three males with situs ambiguous. - - Familial - - - - - Aimee Paulussen 00059077
0000045668 Heterotaxy, VSD, L hip dysplasia. - - Familial - - - - - Aimee Paulussen 00059078
0000045669 Two male brothers with situs ambiguous and anal malformations. - - Familial - - - - - Aimee Paulussen 00059079
0000045670 Abdominal situs inversus, asplenia, CAVC, PA, d-TGA. - - Familial - - - - - Aimee Paulussen 00059080
0000045671 - - - Unknown - - - - - Aimee Paulussen 00059081
0000045672 Situs ambiguous, sacral agenesis. - - Familial - - - - - Aimee Paulussen 00059082
0000045673 d-TGA, single ventricle, PA, polysplenia. - - Familial - - - - - Aimee Paulussen 00059083
0000045674 HLHS, right atrial isomerism, TGA, aplenia, malrotation webbed neck, abnormal liver lobation. - - Familial - - - - - Aimee Paulussen 00059084
0000045675 Asplenia, CAVC, PA. - - Familial - - - - - Aimee Paulussen 00059085
0000045676 Single ventricle, PS, DORV, asplenia, horseshoe kidney, low-set ears, abnormal situs. - - Familial - - - - - Aimee Paulussen 00059086
0000045677 Hypoplastic LV, d-TGA, DORV, VSD, ventricular inversion, heterotaxy, gut malrotation, polysplenia, midline liver. - - Familial - - - - - Aimee Paulussen 00059087
0000045678 Isolated CHD, HLHS, PS, l-TGA, DILV, ASD, DORV, heterotaxy, dextrocardia, d-TGA, TA. - - Familial - - - - - Aimee Paulussen 00059088
0000045679 d-TGA - - Unknown - - - - - Aimee Paulussen 00059089
0000045683 ASD type II, VSD, AVSD, situs inversus totalis, dextrocardia. - - Familial - - - - - Aimee Paulussen 00059093
0000045684 - - - Unknown - - - - - Aimee Paulussen 00059094
0000045685 Dextroposition heart, bilat superior vena cava, oesophageal atresia, anal atresia, multicystic dysplasia. - - Unknown - - - - - Aimee Paulussen 00059095
0000045686 Heterotaxy - - Unknown - - - - - Aimee Paulussen 00059096
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.