ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

7 OMIM references -
7 associated genes
No signs/symptoms info

Syndromic microphthalmia type 5

Isolated anophthalmia - microphthalmia

Citations in the biomedical literature:

Syndromic microphthalmia type 5		Isolated anophthalmia - microphthalmia
	Synonym(s): - MCOPS5 - Syndromic microphthalmia/anophthalmia due to OTX2 mutation		Synonym(s): - Clinical anophthalmia - Isolated pure microphthalmia - Primitive anophthalmia

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

	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: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 7 OMIM references - No MeSH references

No signs/symptoms info available.