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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
9 OMIM references -
8 associated genes
No signs/symptoms info
Postaxial polydactyly type B, unilateral
Colobomatous microphthalmia

GLI3 ABCB6
GDF3
GDF6
SHH
SOX2
STRA6
TENM3
VSX2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
GLI3
(0.63)
SOX2



Citations in the biomedical literature:


Postaxial polydactyly type B, unilateral
GLI3
Colobomatous microphthalmia
ABCB6 GDF3 GDF6 SHH SOX2 STRA6
TENM3 VSX2



Postaxial polydactyly type B, unilateral
Colobomatous microphthalmia

Synonym(s):
(no synonyms)

Synonym(s):
- MAC
- Microphthalmia - anophthalmia - coloboma
- Microphthalmia with colobomatous cyst

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

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

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
9 OMIM references -
No MeSH references

No signs/symptoms info available.