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Disease association ontology term - MONDO:0019600 - xeroderma pigmentosum

Term summary

ID
MONDO:0019600
Name
xeroderma pigmentosum
Ontology or CV name
Disease association
Definition
Xeroderma pigmentosum (XP) is a rare genodermatosis characterized by extreme sensitivity to ultraviolet (UV)-induced changes in the skin and eyes, and multiple skin cancers. It is subdivided into 8 complementation groups, according to the affected gene: classical XP (XPA to XPG) and XP variant (XPV).

Parents

Annotation

Disease association

MONDO:0019600 - xeroderma pigmentosum

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Genes:

MONDO:0010210 - xeroderma pigmentosum group A

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MONDO:0012531 - xeroderma pigmentosum group B

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MONDO:0010211 - xeroderma pigmentosum group C

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MONDO:0010212 - xeroderma pigmentosum group D

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MONDO:0010215 - xeroderma pigmentosum group F

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MONDO:0010216 - xeroderma pigmentosum group G

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MONDO:0010214 - xeroderma pigmentosum variant type

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MONDO:0980987 - xeroderma pigmentosum, complementation group J

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