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

Athabaskan brainstem dysgenesis syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PRNP	(0.78)	HOXA1

Citations in the biomedical literature:

Inherited Creutzfeldt-Jakob disease		Athabaskan brainstem dysgenesis syndrome
	Synonym(s): - Inherited CJD		Synonym(s): - ABSD - Athabascan brainstem dysgenesis syndrome - Navajo brainstem syndrome

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

	Classification (ICD10): - Certain infectious and parasitic diseases -		Classification (ICD10): (no data available)

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: no data available Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C535397

No signs/symptoms info available.