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Isolated scaphocephaly

3 OMIM references -
3 associated genes
5 signs/symptoms

COMMON GENES: 1

Parietal foramina

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

Isolated scaphocephaly

Parietal foramina

ALX4	(UniProt - OMIM)		ALX4	(UniProt - OMIM)
ERF	(UniProt - OMIM)		MSX2	(UniProt - OMIM)
TWIST1	(UniProt - OMIM)


COMMON GENES	ALX4

Citations in the biomedical literature:

Isolated scaphocephaly		Parietal foramina
	Synonym(s): - Isolated dolichocephaly - Non-syndromic sagittal synostosis		Synonym(s): - Catlin marks - Enlarged parietal foramina - Foramina parietalia permagna - Hereditary cranium bifidum

	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): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 3 OMIM references - No MeSH references		External references: 3 OMIM references - No MeSH references

Isolated scaphocephaly
	Very frequent - Dolichocephaly / scaphocephaly Occasional - Autosomal dominant inheritance - Cranial hypertension - Frontal bossing / prominent forehead - Prominent occiput / occipital bossing
Parietal foramina
(no data available)