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Situs ambiguus
6 associated genes
42 connected diseases
No signs/symptoms info
Disease Type of connection
Double outlet right ventricle
Situs inversus totalis
Alobar holoprosencephaly
Biliary atresia with splenic malformation syndrome
Isolated congenitally uncorrected transposition of the great arteries
Lobar holoprosencephaly
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
Hereditary hemorrhagic telangiectasia
Brachydactyly type A2
Ovarian adenocarcinoma
Acrocallosal syndrome
Greig cephalopolysyndactyly syndrome
Pallister-Hall syndrome
Polysyndactyly, bilateral
Polysyndactyly, unilateral
Postaxial polydactyly type A, bilateral
Postaxial polydactyly type A, unilateral
Postaxial polydactyly type B, bilateral
Postaxial polydactyly type B, unilateral
Myostatin-related muscle hypertrophy
Acromesomelic dysplasia, Grebe type
Acromesomelic dysplasia, Hunter-Thomson type
Angel-shaped phalango-epiphyseal dysplasia
Brachydactyly type A1
Brachydactyly type C
Fibular aplasia - complex brachydactyly
Multiple synostoses syndrome
Proximal symphalangism
Familial cerebral saccular aneurysm
Generalized juvenile polyposis / juvenile polyposis coli
X-linked central congenital hypothyroidism with late-onset testicular enlargement
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
20p12.3 microdeletion syndrome
- Incomplete situs inversus
- Partial situs inversus
- Situs ambiguous

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare surgical cardiac disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.