ODCs

Click node...

2 OMIM references -
2 associated genes
7 signs/symptoms

PROTEIN INTERACTIONS: 1

2 associated genes
No signs/symptoms info

Isolated trigonocephaly

Acute myeloid leukemia with t(8;16)(p11;p13) translocation

FGFR1	(UniProt - OMIM)		CREBBP	(UniProt - OMIM)
FREM1	(UniProt - OMIM)		KAT6A	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FGFR1	(0.67)	CREBBP

Citations in the biomedical literature:

Isolated trigonocephaly		Acute myeloid leukemia with t(8;16)(p11;p13) translocation
	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 hematologic 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: (no data available)

	External references: 2 OMIM references - No MeSH references		External references: No 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
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
(no data available)