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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
7 signs/symptoms
Pilomatrixoma
Craniorachischisis

CTNNB1 DACT1


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Pilomatrixoma
CTNNB1
Craniorachischisis
DACT1



Pilomatrixoma
Craniorachischisis

Synonym(s):
- Epithelioma calcificans of Malherbe
- Pilomatricoma

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease

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

Epidemiological data:
(no data available)
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

External references:
1 OMIM reference -
1 MeSH reference: D018296
External references:
No OMIM references
No MeSH references

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


Pilomatrixoma

(no data available)