Situs inversus totalis

Symptom Information:

Symptom ID: HPO:0001696
Synonyms:
Situs inversus [HPO:0001696]
situs oppositus [HPO:0001696]
situs transversus [HPO:0001696]
Situs inversus visceralis [Orphanet:26560]
Situs inversus viscerum (disorder) [Orphanet:26560]
Situs inversus [OMIM:Situs inversus]
Situs inversus visceralis/colon/intestine trasposition/heterotaxia [Orphanet:26560]
Situs inversus (in 1 family) [OMIM:Situs inversus (in 1 family)]
Situs inversus (in about 50% of patients) [OMIM:Situs inversus (in about 50% of patients)]
Situs inversus (in about half of patients) [OMIM:Situs inversus (in about half of patients)]
Situs inversus (in some patients) [OMIM:Situs inversus (in some patients)]
Situs inversus (rare) [OMIM:Situs inversus (rare)]
Situs inversus (uncommon) [OMIM:Situs inversus (uncommon)]
Situs inversus (variable) [OMIM:Situs inversus (variable)]
Situs inversus totalis (rare) [OMIM:Situs inversus totalis (rare)]
Quality:
Cross references:
HPO:0003363 "Abdominal situs inversus" [Orphanet:26560]
Orphanet:26560 "Situs inversus visceralis/colon/intestine trasposition/heterotaxia" [Orphanet:26560]
OMIM: "Situs inversus" [OMIM:Situs inversus]
OMIM: "Situs inversus (in 1 family)" [OMIM:Situs inversus (in 1 family)]
OMIM: "Situs inversus (in about 50% of patients)" [OMIM:Situs inversus (in about 50% of patients)]
OMIM: "Situs inversus (in about half of patients)" [OMIM:Situs inversus (in about half of patients)]
OMIM: "Situs inversus (in some patients)" [OMIM:Situs inversus (in some patients)]
OMIM: "Situs inversus (rare)" [OMIM:Situs inversus (rare)]
OMIM: "Situs inversus (uncommon)" [OMIM:Situs inversus (uncommon)]
OMIM: "Situs inversus (variable)" [OMIM:Situs inversus (variable)]
OMIM: "Situs inversus totalis (rare)" [OMIM:Situs inversus totalis (rare)]
Is a (Direct Parents):
Orphanet Abnormality of the small intestine
HPO         Abnormal spatial orientation of the cardiac segments
HPO         Dextrocardia
HPO         Abdominal situs inversus
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)