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Isolated trigonocephaly

2 OMIM references -
2 associated genes
7 signs/symptoms

COMMON GENES: 1

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

Isolated trigonocephaly

BNAR syndrome

FGFR1	(UniProt - OMIM)		FREM1	(UniProt - OMIM)
FREM1	(UniProt - OMIM)


COMMON GENES	FREM1

Citations in the biomedical literature:

Isolated trigonocephaly		BNAR syndrome
	Synonym(s): - Non-syndromic metopic craniosynostosis		Synonym(s): - Bifid nose with or without anorectal and renal anomalies

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease		Classification (Orphanet): - Rare abdominal surgical disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare otorhinolaryngologic disease - Rare renal disease

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

	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 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

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

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