ODCs

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

PROTEIN INTERACTIONS: 1

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

Parietal foramina

Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome

ALX4	(UniProt - OMIM)		ALX1	(UniProt - OMIM)
MSX2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ALX4	(0.52)	ALX1

Citations in the biomedical literature:

Parietal foramina		Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome
	Synonym(s): - Catlin marks - Enlarged parietal foramina - Foramina parietalia permagna - Hereditary cranium bifidum		Synonym(s): - ALX1-related frontonasal dysplasia

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare maxillo-facial surgical disease - Rare otorhinolaryngologic 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: - 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: 3 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.