ODCs

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

PROTEIN INTERACTIONS: 1

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

Hereditary spherocytosis

Xeroderma pigmentosum complementation group F


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SPTA1	(0.72)	ERCC4

Citations in the biomedical literature:

Hereditary spherocytosis		Xeroderma pigmentosum complementation group F
	Synonym(s): - Minkowski-Chauffard disease		Synonym(s): - XPF

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare oncologic disease - Rare otorhinolaryngologic disease - Rare skin 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: Class of prevalence: 1-5 / 10 000 Average age onset: variable Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive

	External references: 4 OMIM references - 2 MeSH references: C536356 / D013103		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.