Abdominal situs inversus

Symptom Information:

Symptom ID: HPO:0003363
Synonyms:
Situs inversus visceralis [HPO:0003363]
Situs inversus viscerum [HPO:0003363]
Situs inversus visceralis [Orphanet:26560]
Situs inversus viscerum (disorder) [Orphanet:26560]
Situs inversus viscerum [OMIM:Situs inversus viscerum]
Situs inversus visceralis/colon/intestine trasposition/heterotaxia [Orphanet:26560]
Quality:
Cross references:
HPO:0001696 "Situs inversus totalis" [Orphanet:26560]
Orphanet:26560 "Situs inversus visceralis/colon/intestine trasposition/heterotaxia" [Orphanet:26560]
OMIM: "Situs inversus viscerum" [OMIM:Situs inversus viscerum]
Is a (Direct Parents):
HPO         Abnormality of abdominal situs
Orphanet Abnormality of the small intestine
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)
MedDRA:
Database Frequency: 19 / 7739
Resource:

All diseases associated with this symptom:

Agnathia - holoprosencephaly - situs inversus (Orphanet:990)
Alport syndrome (Orphanet:63)
Colonic atresia (Orphanet:1198)
Congenital pseudoarthrosis of clavicle (Orphanet:66630)
Diabetic embryopathy (Orphanet:1926)
Familial long QT syndrome (Orphanet:768)
Familial visceral myopathy (Orphanet:2604)
HETEROTAXY, VISCERAL, 1, X-LINKED (OMIM:306955)
HETEROTAXY, VISCERAL, 2, AUTOSOMAL (OMIM:605376)
HETEROTAXY, VISCERAL, 5, AUTOSOMAL (OMIM:270100)
HETEROTAXY, VISCERAL, 6, AUTOSOMAL (OMIM:614779)
Hallermann-Streiff syndrome (Orphanet:2108)
Heterotaxia (Orphanet:450)
Progressive non-infectious anterior vertebral fusion (Orphanet:2062)
Renpenning syndrome (Orphanet:3242)
Sacrococcygeal dysgenesis association (Orphanet:1773)
Short rib-polydactyly syndrome (Orphanet:1505)
Thiamine-responsive megaloblastic anemia syndrome (Orphanet:49827)
Wolf-Hirschhorn syndrome (Orphanet:280)