ODCs

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

PROTEIN INTERACTIONS: 1

3 associated genes
No signs/symptoms info

Combined immunodeficiency due to STK4 deficiency

Myxofibrosarcoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	STK4	(0.63)	FUS

Citations in the biomedical literature:

Combined immunodeficiency due to STK4 deficiency		Myxofibrosarcoma
	Synonym(s): - CID due to STK4 deficiency		Synonym(s): - Fibromyxosarcoma - Myxoid malignant fibrous histiocytoma

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

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: sporadic

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

No signs/symptoms info available.