Cytoscape Web
Click node...

Isolated Dandy-Walker malformation with hydrocephalus
2 associated genes
17 connected diseases
No signs/symptoms info
Disease Type of connection
Isolated Dandy-Walker malformation without hydrocephalus
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
Alobar holoprosencephaly
Combined pituitary hormone deficiencies, genetic forms
Lobar holoprosencephaly
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic 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
ZIC1 Q15915600470
ZIC4 Q8N9L1608948
No signs/symptoms info available.