ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Severe combined immunodeficiency due to DNA-PKcs deficiency

Isolated adermatoglyphia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PRKDC	(0.63)	SMARCAD1

Citations in the biomedical literature:

Severe combined immunodeficiency due to DNA-PKcs deficiency		Isolated adermatoglyphia
	Synonym(s): - SCID due to DNA-PKcs deficiency		Synonym(s): - Absence of fingerprints - Immigration delay disease

	Classification (Orphanet): - Rare genetic disease - Rare immune disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic 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: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant

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

No signs/symptoms info available.