ODCs

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

PROTEIN INTERACTIONS: 1

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

Retinitis punctata albescens

Young adult-onset distal hereditary motor neuropathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RHO	(0.65)	DNAJB2

Citations in the biomedical literature:

Retinitis punctata albescens		Young adult-onset distal hereditary motor neuropathy
	Synonym(s): (no synonyms)		Synonym(s): - Autosomal recessive distal spinal muscular atrophy type 5 - Young adult-onset dHMN - dSMA5

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

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

	Epidemiological data: Class of prevalence: - Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.