ODCs

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2 OMIM references -
2 associated genes
7 signs/symptoms

COMMON GENES: 1

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

Isolated trigonocephaly

Myeloid neoplasm associated with FGFR1 rearrangement

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

Citations in the biomedical literature:

Isolated trigonocephaly		Myeloid neoplasm associated with FGFR1 rearrangement
	Synonym(s): - Non-syndromic metopic craniosynostosis		Synonym(s): - 8p11 myeloproliferative syndrome - Stem cell leukemia/lymphoma

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): (no data available)

	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: (no data available)

	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
Myeloid neoplasm associated with FGFR1 rearrangement
(no data available)