Cytoscape Web
Click node...

Occipital encephalocele
1 associated gene
11 connected diseases
No signs/symptoms info
Disease Type of connection
Craniorachischisis
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
17p13.3 microduplication syndrome
Burkitt lymphoma
Distal 17p13.3 microdeletion syndrome
Miller-Dieker syndrome
Precursor T-cell acute lymphoblastic leukemia
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
DACT1 Q9NYF0607861
No signs/symptoms info available.