ODCs

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

PROTEIN INTERACTIONS: 1

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

Atypical Gaucher disease due to saposin C deficiency

Synaptic congenital myasthenic syndromes

PSAP	(UniProt - OMIM)		COLQ	(UniProt - OMIM)
			LAMB2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PSAP	(0.63)	LAMB2

Citations in the biomedical literature:

Atypical Gaucher disease due to saposin C deficiency		Synaptic congenital myasthenic syndromes

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: (no data available)		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.