Situs inversus totalis
Symptom Information:
Symptom ID: | HPO:0001696 | |||||||||||||||
Synonyms: |
|
|||||||||||||||
Quality: | ||||||||||||||||
Cross references: |
|
|||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the abdomen(HPO:0001438) Abnormality of abdominal situs(HPO:0011620) Abdominal situs inversus(HPO:0003363) Situs inversus totalis(HPO:0001696) Abnormality of the cardiovascular system(HPO:0001626) Abnormal heart morphology(HPO:0001627) obsolete Malformation of the heart and great vessels(HPO:0002564) Abnormal spatial orientation of the cardiac segments(HPO:0011534) Situs inversus totalis(HPO:0001696) Abnormal anatomic location of the heart(HPO:0004307) Dextrocardia(HPO:0001651) Situs inversus totalis(HPO:0001696) MedDRA: |
|||||||||||||||
Database Frequency: | 44 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
Agnathia - holoprosencephaly - situs inversus | (Orphanet:990) |
Bardet-Biedl syndrome 17 | (OMIM:615994) |
Bardet-Biedl syndrome 8 | (OMIM:615985) |
CARPENTER SYNDROME 2 | (OMIM:614976) |
CILIARY DYSKINESIA, PRIMARY, 1 | (OMIM:244400) |
CILIARY DYSKINESIA, PRIMARY, 10 | (OMIM:612518) |
CILIARY DYSKINESIA, PRIMARY, 13 | (OMIM:613193) |
CILIARY DYSKINESIA, PRIMARY, 14 | (OMIM:613807) |
CILIARY DYSKINESIA, PRIMARY, 15 | (OMIM:613808) |
CILIARY DYSKINESIA, PRIMARY, 16 | (OMIM:614017) |
CILIARY DYSKINESIA, PRIMARY, 17 | (OMIM:614679) |
CILIARY DYSKINESIA, PRIMARY, 18 | (OMIM:614874) |
CILIARY DYSKINESIA, PRIMARY, 19 | (OMIM:614935) |
CILIARY DYSKINESIA, PRIMARY, 2 | (OMIM:606763) |
CILIARY DYSKINESIA, PRIMARY, 20 | (OMIM:615067) |
CILIARY DYSKINESIA, PRIMARY, 22 | (OMIM:615444) |
CILIARY DYSKINESIA, PRIMARY, 23 | (OMIM:615451) |
CILIARY DYSKINESIA, PRIMARY, 25 | (OMIM:615482) |
CILIARY DYSKINESIA, PRIMARY, 26 | (OMIM:615500) |
CILIARY DYSKINESIA, PRIMARY, 28 | (OMIM:615505) |
CILIARY DYSKINESIA, PRIMARY, 3 | (OMIM:608644) |
CILIARY DYSKINESIA, PRIMARY, 30 | (OMIM:616037) |
CILIARY DYSKINESIA, PRIMARY, 7 | (OMIM:611884) |
CILIARY DYSKINESIA, PRIMARY, 9 | (OMIM:612444) |
Diabetic embryopathy | (Orphanet:1926) |
Familial long QT syndrome | (Orphanet:768) |
Isolated congenital hypoglossia/aglossia | (Orphanet:141152) |
Ivemark syndrome | (Orphanet:97548) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
LATERALITY DEFECTS, AUTOSOMAL DOMINANT | (OMIM:601086) |
MARFANOID HABITUS WITH SITUS INVERSUS | (OMIM:609008) |
Meckel syndrome, type 4 | (OMIM:611134) |
Nephronophthisis 12 | (OMIM:613820) |
Nephronophthisis 14 | (OMIM:614844) |
Nephronophthisis 16 | (OMIM:615382) |
Nephronophthisis 2 | (OMIM:602088) |
Nephronophthisis 3 | (OMIM:604387) |
Nephronophthisis 9 | (OMIM:613824) |
Porencephaly - cerebellar hypoplasia - internal malformations | (Orphanet:2941) |
RENAL-HEPATIC-PANCREATIC DYSPLASIA 2 | (OMIM:615415) |
RETINITIS PIGMENTOSA WITH OR WITHOUT SITUS INVERSUS | (OMIM:615434) |
Renpenning syndrome | (Orphanet:3242) |
SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE | (OMIM:613686) |
Thiamine-responsive megaloblastic anemia syndrome | (Orphanet:49827) |