ODCs

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

PROTEIN INTERACTIONS: 1

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

Inherited Creutzfeldt-Jakob disease

X-linked myopathy with postural muscle atrophy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PRNP	(0.68)	FHL1

Citations in the biomedical literature:

Inherited Creutzfeldt-Jakob disease		X-linked myopathy with postural muscle atrophy
	Synonym(s): - Inherited CJD		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Certain infectious and parasitic diseases -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: - Average age of death: - Type of inheritance: x-linked recessive

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

No signs/symptoms info available.