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1 OMIM reference -
6 associated genes
12 signs/symptoms
COMMON GENES: 1
COMMON SIGNS: 3
1 OMIM reference -
1 associated gene
7 signs/symptoms
Peters anomaly
Foveal hypoplasia - presenile cataract

CYP1B1 PAX6
FOXC1
HDAC9
PAX6
PITX2
TGFB2


COMMON
GENES
PAX6



Citations in the biomedical literature:


Peters anomaly
CYP1B1 FOXC1 HDAC9 PAX6 PITX2 TGFB2

Foveal hypoplasia - presenile cataract



Peters anomaly
Foveal hypoplasia - presenile cataract

Synonym(s):
- Peters congenital glaucoma

Synonym(s):
- O'Donnell-Pappas syndrome

Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the eye and adnexa -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
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: adulthood
Average age of death: normal
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: C537884
External references:
1 OMIM reference -
No MeSH references


COMMON
SIGNS
- Anomalies of eyes and vision
- Cataract / lens opacification
- Nystagmus


Peters anomaly
Foveal hypoplasia - presenile cataract

Very frequent
- Autosomal recessive inheritance
- Microcornea

Frequent
- Corneal dystrophy

Occasional
- Anomalies of teeth and dentition
- Anophthalmos / anophthalmia / microphthalmos / microphthalmia
- Aphakia / microphakia / spherophakia / biphakia / absence of lens / lenticone / lentiglobus
- Corneal clouding / opacity / vascularisation
- Dental malocclusion
- Hypoplastic mandibula / partial absence of the mandibula


Very frequent
- Autosomal dominant inheritance
- Diffuse / generalised skin hyperpigmentation / melanoderma
- Optic nerve anomaly / optic atrophy / anomaly of the papilla

Frequent
- Strabismus / squint