visceral heterotaxy

rare disease
rdfs:label
"visceral heterotaxy"@en
skos:altLabel
"HETEROTAXY, VISCERAL, 2, AUTOSOMAL"@en
"HETEROTAXY, VISCERAL, 2, AUTOSOMAL; HTX2"@en
"HTX2"@en
"Heterotaxy Syndrome"@en
"Htx"@en
"Incomplete situs inversus"@en
"Partial situs inversus"@en
"Situs ambiguous"@en
"Transposition of the Great Arteries, Dextro-Looped 2; DTGA2"@en
"heterotaxia"@en
"situs ambiguus"@en
schema:description
"rare disease"@en
schema:dateModified "2026-09-29T19:49:19+00:00"^^xsd:dateTime
schema:version 2550980281
wikibase:identifiers 28
wikibase:sitelinks 6
wikibase:statements 47
p:P11430 wd:statement/Q203115-e0c74ae9-42d8-1572-bc37-240d58409865
p:P1550 wd:statement/Q203115-28CF1E27-181E-437D-ABE8-3453DFAF15B1
wd:statement/Q203115-DCB04526-61FF-4BEB-AB3B-9C5C13B63807
p:P1748 wd:statement/Q203115-781F7009-19C3-4134-B04C-94679C19D66F
p:P1995 wd:statement/Q203115-853E90F4-63A6-4F83-9051-148D89F64BBF
wd:statement/Q203115-B4A31257-9CD6-48B6-B82F-887E62A2B01B
p:P2293 wd:statement/Q203115-040EF581-0C6F-4A3C-9F77-9964D4F4F7F5
wd:statement/Q203115-3A85F045-01EA-4A7B-B759-DC87CA84D50B
wd:statement/Q203115-52F207E2-2731-4D1C-ACD3-6260C924F617
wd:statement/Q203115-69B62E77-058D-499A-BD01-D6F3746A51E5
p:P279 wd:statement/Q203115-5062B00B-5B19-4BB5-BCCC-8A125A4EA77E
wd:statement/Q203115-70FB26E1-ACA3-46FF-BAA9-A58B20619D6C
wd:statement/Q203115-9CAEBFE3-9109-47D9-A544-93FBC7ADB7DE
wd:statement/Q203115-FC88C2A2-86C3-48F8-8FEF-29CCE5C1ABA6
p:P2888 wd:statement/Q203115-4AC50C03-E0AD-4F53-80E6-02222FDE69A9
wd:statement/Q203115-8B3DAA87-BA26-406C-82FB-2F89E444D7C6
wd:statement/Q203115-8E10F1C3-6B97-42C2-BDB6-4564E682E898
wd:statement/Q203115-AB671300-C8FC-4CB9-A4DD-7DA32B4A6CDC
wd:statement/Q203115-B06594CE-A969-43F4-96FE-B266A8E99ADF
p:P2892 wd:statement/Q203115-06653269-24F9-4A6A-A8A6-1F60EE676AC5
wd:statement/Q203115-2CE81B5E-C6BF-4032-B1A0-ABB1571CBB02
wd:statement/Q203115-577A8470-25F5-4DE5-9822-3EF7F261C917
wd:statement/Q203115-810C51CB-26DC-4B9B-8C09-35CB7FCCD2E3
wd:statement/Q203115-E375B384-1987-49EA-86D2-45AABE019D49
wd:statement/Q203115-EA0A3C41-A0AB-41BF-B500-10C74A7BEBE2
p:P31 wd:statement/Q203115-BF4252E8-1938-476F-B18D-7D547DF22502
wd:statement/Q203115-D9F0FDA4-0417-4CD7-A512-FF9AD68D1CB4
p:P3841 wd:statement/Q203115-D7A674C9-7AC3-44FC-B8E2-77E3A6FA24F8
p:P4229 wd:statement/Q203115-53FA48BE-F327-40BD-BE44-F6FB0F970AD1
p:P4317 wd:statement/Q203115-8CFAEFDF-6E7C-49FE-800C-DCDC032B7FC8
p:P486 wd:statement/Q203115-C41D886A-F422-490C-94E0-7E1246C2EB2D
p:P492 wd:statement/Q203115-03014714-B985-426D-A08B-C2B0BE6089A7
wd:statement/Q203115-175D1B4C-EDFC-495B-B3CF-5B429B0BD1BF
wd:statement/Q203115-6BFF394A-A22C-4FE4-882F-0BC657260F2C
wd:statement/Q203115-9AC97018-C3E2-41A2-B38D-8F7706972BB1
wd:statement/Q203115-C2B33AF6-BF17-48E8-9CA6-8AA3AD7D55F2
p:P5008 wd:statement/Q203115-818F9063-FAF0-42A5-A018-52AA3F86CC5A
p:P5270 wd:statement/Q203115-182B39EA-BC5E-4F93-8CC3-44E683028E5E
p:P646 wd:statement/Q203115-8C3134D1-D406-4A81-A0B2-C1B421FE0F4C
p:P665 wd:statement/Q203115-D5B102C8-7C7A-4775-A040-B9E6C661C83E
p:P672 wd:statement/Q203115-06E779F9-453B-4145-8C3F-C25AC17DE2DC
wd:statement/Q203115-0DEE3C79-7D7D-48F1-958E-8FA16523A09B
wd:statement/Q203115-36DE0442-6683-46BF-9043-92BFE3C6BE72
wd:statement/Q203115-37C0E568-35A3-4B43-9BA5-AAC87874E13A
wd:statement/Q203115-F15D4ECB-0D12-413B-A6EB-180E59758040
p:P699 wd:statement/Q203115-C65F3E92-99D4-4E9B-8BAD-C35259DD6502
p:P7807 wd:statement/Q203115-28A27C90-2C15-4111-852F-4AAB19CFEFC5
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D059446>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0015522>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00632>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C14.240.400.592>
<http://id.nlm.nih.gov/mesh/C14.280.400.592>
<http://id.nlm.nih.gov/mesh/C15.604.744.146>
<http://id.nlm.nih.gov/mesh/C16.131.077.401>
<http://id.nlm.nih.gov/mesh/C16.131.240.400.592>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0050545>
wdt:P11430 "DI-02413"
wdt:P1550 "157769"
"450"
wdt:P1748 "C87083"
wdt:P1995 cardiology
angiology
wdt:P2293 ACVR2B
CFC1
ZIC3
CFAP53
wdt:P279 genetic cardiac anomaly
developmental defect during embryogenesis
wdt:P2888 <http://identifiers.org/doid/DOID:0050545>
<http://purl.obolibrary.org/obo/DOID_0050545>
<http://purl.obolibrary.org/obo/HP_0011536>
<http://www.orpha.net/ORDO/Orphanet_157769>
<http://www.orpha.net/ORDO/Orphanet_450>
wdt:P2892 "C0266642"
"C1167664"
"C1415817"
"C1854334"
"C3178805"
"C3178806"
wdt:P31 type of disease
rare disease
wdt:P3841 "HP:0011536"
wdt:P4229 "Q89.3"
wdt:P4317 "10875"
wdt:P486 "D059446"
wdt:P492 "306955"
"605376"
"606325"
"613751"
"614779"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0015522"
wdt:P646 "/m/043c5p"
wdt:P665 "H00632"
wdt:P672 "C14.240.400.592"
"C14.280.400.592"
"C15.604.744.146"
"C16.131.077.401"
"C16.131.240.400.592"
wdt:P699 "DOID:0050545"
wdt:P7807 "780273165"
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