ODCs

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2 OMIM references -
2 associated genes
7 signs/symptoms

PROTEIN INTERACTIONS: 1

2 OMIM references -
2 associated genes
No signs/symptoms info

Isolated trigonocephaly

Nodulosis-arthropathy-osteolysis syndrome

FGFR1	(UniProt - OMIM)		MMP14	(UniProt - OMIM)
FREM1	(UniProt - OMIM)		MMP2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FGFR1	(0.55)	MMP2

Citations in the biomedical literature:

Isolated trigonocephaly		Nodulosis-arthropathy-osteolysis syndrome
	Synonym(s): - Non-syndromic metopic craniosynostosis		Synonym(s): - Multicentric osteolysis - nodulosis - arthropathy - NAO syndrome

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the musculoskeletal system and connective tissue -

	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: 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
Nodulosis-arthropathy-osteolysis syndrome
(no data available)