ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
12 signs/symptoms

Severe combined immunodeficiency due to DNA-PKcs deficiency

Familial partial lipodystrophy due to AKT2 mutations


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PRKDC	(0.75)	AKT2

Citations in the biomedical literature:

Severe combined immunodeficiency due to DNA-PKcs deficiency		Familial partial lipodystrophy due to AKT2 mutations
	Synonym(s): - SCID due to DNA-PKcs deficiency		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare immune disease		Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

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

	External references: No OMIM references No MeSH references		External references: No OMIM references No MeSH references

Familial partial lipodystrophy due to AKT2 mutations
	Very frequent - Abnormal fat distribution / lipodystrophy - Autosomal dominant inheritance - Chronic arterial hypertension - Hyperlipidemia / hypercholesterolemia / hypertriglyceridemia - Insulin resistance - Insulin-dependent / type 1 diabetes Frequent - Abnormal / polycystic ovaries - Acanthosis nigricans - Liver / hepatic steatosis Occasional - Angor pectoris / myocardial infarction - Arterial atheroma / precocious atherosclerosis / arteriosclerosis - Heart / cardiac failure
Severe combined immunodeficiency due to DNA-PKcs deficiency
(no data available)