ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
3 signs/symptoms

Autosomal recessive lymphoproliferative disease

X-linked severe congenital neutropenia

CD27	(UniProt - OMIM)		WAS	(UniProt - OMIM)
ITK	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ITK	(0.86)	WAS

Citations in the biomedical literature:

Autosomal recessive lymphoproliferative disease		X-linked severe congenital neutropenia

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

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

	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: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: x-linked recessive

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

X-linked severe congenital neutropenia
	Very frequent - Agammaglobulinemia / hypogammaglobulinemia / B-cell deficiency - Polynuclear cells / neutrophils anomalies / neutropenia - X-linked recessive inheritance
Autosomal recessive lymphoproliferative disease
(no data available)