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Postaxial polydactyly type B, unilateral
1 associated gene
48 connected diseases
No signs/symptoms info
Disease Type of connection
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
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Alobar holoprosencephaly
Isolated Dandy-Walker malformation with hydrocephalus
Isolated Dandy-Walker malformation without hydrocephalus
Lobar holoprosencephaly
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
1p36 deletion syndrome
Shprintzen-Goldberg syndrome
Double outlet right ventricle
Isolated congenitally uncorrected transposition of the great arteries
Situs ambiguus
Split hand-split foot malformation
Desmoplastic / nodular medulloblastoma
Familial multiple meningioma
Medulloblastoma with extensive nodularity
Blepharophimosis-intellectual deficit syndrome, MKB type
FG syndrome type 1
X-linked intellectual deficit with marfanoid habitus
X-linked non-syndromic intellectual deficit
17p13.3 microduplication syndrome
Anophthalmia / microphthalmia - esophageal atresia
Colobomatous microphthalmia
Distal 17p13.3 microdeletion syndrome
Isolated anophthalmia - microphthalmia
Miller-Dieker syndrome
Septo-optic dysplasia
Aneurysm - osteoarthritis syndrome
Familial pancreatic carcinoma
Familial thoracic aortic aneurysm and aortic dissection
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
Isolated brachycephaly
Isolated scaphocephaly
Myhre syndrome
Saethre-Chotzen syndrome
(no synonyms)

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

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

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

Gene symbol UniProt reference OMIM reference
GLI3 P10071165240
No signs/symptoms info available.