ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

6 OMIM references -
4 associated genes
No signs/symptoms info

Familial isolated congenital asplenia

Hereditary breast cancer


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RPSA	(0.52)	BRCA1

Citations in the biomedical literature:

Familial isolated congenital asplenia		Hereditary breast cancer
	Synonym(s): (no synonyms)		Synonym(s): - Familial breast cancer - Familial breast carcinoma - Hereditary breast carcinoma

	Classification (Orphanet): - Rare abdominal surgical disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare immune disease		Classification (Orphanet): - Rare genetic disease - Rare gynecologic or obstetric disease - Rare oncologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: 6 OMIM references - No MeSH references

No signs/symptoms info available.