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Craniorachischisis

1 associated gene
7 signs/symptoms

PROTEIN INTERACTIONS: 1

Burkitt lymphoma

1 OMIM reference -
1 associated gene
No signs/symptoms info

Craniorachischisis

Burkitt lymphoma

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	DACT1	(0.63)	MYC

Citations in the biomedical literature:

Craniorachischisis		Burkitt lymphoma
	Synonym(s): (no synonyms)		Synonym(s): - Small non-cleaved cell lymphoma

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare hematologic 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: unknown Average age onset: variable Average age of death: any age Type of inheritance: sporadic

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 2 MeSH references: D002051 / D008228

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
Burkitt lymphoma
(no data available)