ODCs

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5 OMIM references -
6 associated genes
No signs/symptoms info

COMMON GENES: 1

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

Achromatopsia

Primary ciliary dyskinesia - retinitis pigmentosa

Citations in the biomedical literature:

Achromatopsia		Primary ciliary dyskinesia - retinitis pigmentosa
	Synonym(s): - ACHM - Complete or incomplete color blindness - Pingelapese blindness - Rod monochromacy - Rod monochromatism - Total color blindness		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare eye disease - Rare genetic disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare respiratory disease

	Classification (ICD10): - Diseases of the eye and adnexa -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: x-linked recessive

	External references: 5 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.