ODCs

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

PROTEIN INTERACTIONS: 1

3 OMIM references -
3 associated genes
No signs/symptoms info

Primary CD59 deficiency

Auriculocondylar syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CD59	(0.55)	GNAI3

Citations in the biomedical literature:

Primary CD59 deficiency		Auriculocondylar syndrome
	Synonym(s): (no synonyms)		Synonym(s): - Question mark ear syndrome

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease - Rare neurologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare maxillo-facial surgical disease - Rare otorhinolaryngologic disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 3 OMIM references - 1 MeSH reference: C538270

No signs/symptoms info available.