ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
3 signs/symptoms

Congenital myopathy with excess of thin filaments

Griscelli disease type 3

ACTA1	(UniProt - OMIM)		MLPH	(UniProt - OMIM)
			MYO5A	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ACTA1	(0.72)	MLPH

Citations in the biomedical literature:

Congenital myopathy with excess of thin filaments		Griscelli disease type 3
	Synonym(s): - Actin myopathy		Synonym(s): - Griscelli-PruniÃ©ras syndrome type 3

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

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

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

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537303

Griscelli disease type 3
	Very frequent - Decreased hair pigmentation / hypopigmentation of hair - Diffuse / generalised skin hypopigmentation / cutaneous albinism Occasional - Iris albinism / ocular albinism
Congenital myopathy with excess of thin filaments
(no data available)