ODCs

Click node...

1 OMIM reference -
3 associated genes
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

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

Fundus albipunctatus

Bothnia retinal dystrophy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RDH5	(0.85)	RLBP1

Citations in the biomedical literature:

Fundus albipunctatus		Bothnia retinal dystrophy
	Synonym(s): (no synonyms)		Synonym(s): - VÃ¤sterbotten dystrophy

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

	Classification (ICD10): - Diseases of the eye and adnexa -		Classification (ICD10): - Diseases of the eye and adnexa -

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

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

No signs/symptoms info available.