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Craniopharyngioma

2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Isolated trigonocephaly

2 OMIM references -
2 associated genes
7 signs/symptoms

Craniopharyngioma

Isolated trigonocephaly

BRAF	(UniProt - OMIM)		FGFR1	(UniProt - OMIM)
CTNNB1	(UniProt - OMIM)		FREM1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CTNNB1	(0.63)	FGFR1

Citations in the biomedical literature:

Craniopharyngioma		Isolated trigonocephaly
	Synonym(s): (no synonyms)		Synonym(s): - Non-syndromic metopic craniosynostosis

	Classification (Orphanet): - Rare endocrine disease - Rare neurologic disease - Rare oncologic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease

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

	Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: variable 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: normal Type of inheritance: autosomal dominant

	External references: No OMIM references 1 MeSH reference: D003397		External references: 2 OMIM references - No MeSH references

Isolated trigonocephaly
	Very frequent - Autosomal dominant inheritance - Trigonocephaly Frequent - Broad nasal root - Hypotelorism - Prominent supraorbital ridge - Synophris / synophrys Occasional - Omphalocele / exomphalos
Craniopharyngioma
(no data available)