ODCs

Click node...

1 OMIM reference -
2 associated genes
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
1 associated gene
3 signs/symptoms

Familial ocular anterior segment mesenchymal dysgenesis

Congenital primary aphakia

FOXE3	(UniProt - OMIM)		FOXE3	(UniProt - OMIM)
PITX3	(UniProt - OMIM)

Citations in the biomedical literature:

Familial ocular anterior segment mesenchymal dysgenesis		Congenital primary aphakia

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

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

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537786

Congenital primary aphakia
	Very frequent - Anomalies of eyes and vision - Anophthalmos / anophthalmia / microphthalmos / microphthalmia - Aphakia / microphakia / spherophakia / biphakia / absence of lens / lenticone / lentiglobus
Familial ocular anterior segment mesenchymal dysgenesis
(no data available)