xeroderma pigmentosum group B
xeroderma pigmentosum characterized by that has material basis in mutation in the ERCC3 gene on chromosome 2q14
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xeroderma pigmentosum group B
Summary
xeroderma pigmentosum group B is a class of disease[1].
Key Facts
- xeroderma pigmentosum group B's instance of is recorded as class of disease[2].
- xeroderma pigmentosum group B's subclass of is recorded as xeroderma pigmentosum[3].
- xeroderma pigmentosum group B's subclass of is recorded as xeroderma pigmentosum-Cockayne syndrome complex[4].
- xeroderma pigmentosum group B's OMIM ID is recorded as 610651[5].
- xeroderma pigmentosum group B's Disease Ontology ID is recorded as DOID:0110850[6].
- xeroderma pigmentosum group B's Orphanet ID is recorded as 276252[7].
- xeroderma pigmentosum group B's NCI Thesaurus ID is recorded as C3966[8].
- xeroderma pigmentosum group B's health specialty is recorded as medical genetics[9].
- xeroderma pigmentosum group B's genetic association is recorded as ERCC3[10].
- xeroderma pigmentosum group B's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110850[11].
- xeroderma pigmentosum group B's exact match is recorded as http://identifiers.org/doid/DOID:0110850[12].
- xeroderma pigmentosum group B's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_220295[13].
- xeroderma pigmentosum group B's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_276252[14].
- xeroderma pigmentosum group B's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_910[15].
- xeroderma pigmentosum group B's UMLS CUI is recorded as C0268136[16].
- xeroderma pigmentosum group B's UMLS CUI is recorded as C1970808[17].
- xeroderma pigmentosum group B's ICD-10-CM is recorded as Q82.1[18].
- xeroderma pigmentosum group B's GARD rare disease ID is recorded as 5625[19].
- xeroderma pigmentosum group B's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
- xeroderma pigmentosum group B's Mondo ID is recorded as MONDO_0012531[21].
- xeroderma pigmentosum group B's UniProt disease ID is recorded as DI-01156[22].