ODCs

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1 OMIM reference -
1 associated gene
5 signs/symptoms

PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1

1 OMIM reference -
6 associated genes
12 signs/symptoms

Dyschromatosis symmetrica hereditaria

Peters anomaly


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ADAR	(0.72)	HDAC9

Citations in the biomedical literature:

Dyschromatosis symmetrica hereditaria		Peters anomaly
	Synonym(s): - Acropigmentation of Dohi		Synonym(s): - Peters congenital glaucoma

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

	Classification (ICD10): - Diseases of the skin and subcutaneous tissue -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood 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 dominant

	External references: 1 OMIM reference - 1 MeSH reference: C535729		External references: 1 OMIM reference - 1 MeSH reference: C537884


COMMON SIGNS	- Autosomal recessive inheritance

Dyschromatosis symmetrica hereditaria		Peters anomaly
	Very frequent - Irregular / in bands / reticular skin hyperpigmentation - Irregular / patchy skin hypopigmentation - Macules Frequent - Dystonia / torticollis / writer's cramp / blepharospasms		Very frequent - Anomalies of eyes and vision - Microcornea Frequent - Corneal dystrophy Occasional - Anomalies of teeth and dentition - Anophthalmos / anophthalmia / microphthalmos / microphthalmia - Aphakia / microphakia / spherophakia / biphakia / absence of lens / lenticone / lentiglobus - Cataract / lens opacification - Corneal clouding / opacity / vascularisation - Dental malocclusion - Hypoplastic mandibula / partial absence of the mandibula - Nystagmus