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Isolated trigonocephaly

2 OMIM references -
2 associated genes
7 signs/symptoms

PROTEIN INTERACTIONS: 1

Craniopharyngioma

2 associated genes
No signs/symptoms info

Isolated trigonocephaly

Craniopharyngioma

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


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

Citations in the biomedical literature:

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

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease		Classification (Orphanet): - Rare endocrine disease - Rare neurologic 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: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: variable Average age of death: - Type of inheritance: sporadic

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

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)