Preferred Name | xeroderma pigmentosum | |
Synonyms |
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Definitions |
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. OMIM mapping confirmed by DO. [SN]. |
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ID |
http://purl.obolibrary.org/obo/DOID_0050427 |
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comment |
OMIM mapping confirmed by DO. [SN]. |
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database_cross_reference |
UMLS_CUI:C0043346 MESH:D014983 SNOMEDCT_US_2023_03_01:44600005 ICD10CM:Q82.1 GARD:7910 NCI:C3452 ORDO:910 |
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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. OMIM mapping confirmed by DO. [SN]. |
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has material basis in | ||
has_obo_namespace |
disease_ontology |
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id |
DOID:0050427 |
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in_subset |
http://purl.obolibrary.org/obo/doid#NCIthesaurus |
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label |
xeroderma pigmentosum |
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notation |
DOID:0050427 |
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note |
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. OMIM mapping confirmed by DO. [SN]. |
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preferred label |
xeroderma pigmentosum |
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prefLabel |
xeroderma pigmentosum |
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subClassOf |