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1 OMIM reference -
6 associated genes
12 signs/symptoms

COMMON GENES: 1
COMMON SIGNS: 2

Morning glory syndrome

1 OMIM reference -
1 associated gene
8 signs/symptoms

Peters anomaly

Morning glory syndrome

CYP1B1	(UniProt - OMIM)		PAX6	(UniProt - OMIM)
FOXC1	(UniProt - OMIM)
HDAC9	(UniProt - OMIM)
PAX6	(UniProt - OMIM)
PITX2	(UniProt - OMIM)
TGFB2	(UniProt - OMIM)


COMMON GENES	PAX6

Citations in the biomedical literature:

Peters anomaly		Morning glory syndrome
	Synonym(s): - Peters congenital glaucoma		Synonym(s): - Ectasic coloboma - Volubilis syndrome

	Classification (Orphanet): (no data available)		Classification (Orphanet): - 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: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: unknown

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


COMMON SIGNS	- Cataract / lens opacification - Nystagmus

Peters anomaly		Morning glory syndrome
	Very frequent - Anomalies of eyes and vision - 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 - Optic nerve anomaly / optic atrophy / anomaly of the papilla - Retinitis pigmentosa / retinal pigmentary changes - Strabismus / squint - Visual loss / blindness / amblyopia Occasional - Coloboma of the optic nerve - Retinal detachment