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Hepatocellular carcinoma, childhood-onset

2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Craniorachischisis

1 associated gene
7 signs/symptoms

Hepatocellular carcinoma, childhood-onset

Craniorachischisis

CTNNB1	(UniProt - OMIM)		DACT1	(UniProt - OMIM)
MET	(UniProt - OMIM)


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

Citations in the biomedical literature:

Hepatocellular carcinoma, childhood-onset		Craniorachischisis

	Classification (Orphanet): - Rare hepatic disease - Rare oncologic 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: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: sporadic		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: No OMIM references No MeSH references		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
Hepatocellular carcinoma, childhood-onset
(no data available)