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DOID:0050427 - xeroderma pigmentosum
Disease Ontology Definition:A syndrome that is characterized by a deficiency in the ability to repair ultraviolet damage that has_material_basis_in autosomal recessive inheritance of DNA repair.
Synonyms:
Xenbase Genes
:
ercc2,
ercc5,
ddb2,
xpa,
ercc4,
xpc,
polh,
ercc6,
ercc3
| MONDO:0019600 - xeroderma pigmentosum |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal recessive disease (is_a),
syndrome (is_a)