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Craniorachischisis

1 associated gene
7 signs/symptoms

PROTEIN INTERACTIONS: 1

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

Craniorachischisis

Pilomatrixoma

(UniProt - OMIM)

(UniProt - OMIM)


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

Citations in the biomedical literature:

Craniorachischisis		Pilomatrixoma
	Synonym(s): (no synonyms)		Synonym(s): - Epithelioma calcificans of Malherbe - Pilomatricoma

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare oncologic disease - Rare skin 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: (no data available)

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

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)