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Craniorachischisis
1 associated gene
7 signs/symptoms
PROTEIN INTERACTIONS: 1
Craniopharyngioma
2 associated genes
No signs/symptoms info
Craniorachischisis
Craniopharyngioma

DACT1
(UniProt - OMIM)
 BRAF
(UniProt - OMIM)
CTNNB1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
DACT1
(0.65)
CTNNB1


Citations in the biomedical literature:


Craniorachischisis
DACT1
Craniopharyngioma
BRAF CTNNB1



Craniorachischisis
Craniopharyngioma

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare neurologic disease
- Rare oncologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: multigenic/multifactorial
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
1 MeSH reference: D003397
Craniorachischisis

Very frequent
- Anencephaly / acrania
- Early death / lethality
- Spina bifida

Occasional
- Diaphragmatic hernia / defect / agenesis
- Imperforate anus / rectum atresia / agenesis / recto-vaginal / vesical / perineal fistula
- Omphalocele / exomphalos
- Sirenomelia / mermaid / lower limb fusion


Craniopharyngioma

(no data available)