Disease #00716 (XPF (xeroderma pigmentosum, complementation group F (XPF)), OMIM:278760)

Official abbreviation XPF
Name xeroderma pigmentosum, complementation group F (XPF)
OMIM ID 278760
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ERCC4
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Individuals

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00073135 - ATX412 - M - France - - 0 - - XPF - ERCC4 ERCC4 1 1 Claire Guissart
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