Xeroderma Pigmentosum, Complementation Group A

Preferred Label : Xeroderma Pigmentosum, Complementation Group A;

NCIt synonyms : XP-A; Xeroderma Pigmentosum Group A; Xeroderma Pigmentosum Complementation Group A;

Details

Origin ID

C3965;

UMLS CUI

C0268135;

Currated CISMeF NLP mapping
- Xeroderma pigmentosum A [ICD-11 More detail]
- Xeroderma pigmentosum complementation group A [ORDO Disease]
- Xeroderma pigmentosum, complementation group a [OMIM Phenotype]
- Xeroderma pigmentosum, group A (disorder) [SNOMED CT concept]
- xeroderma pigmentosum group A [DO Concept]
- xeroderma pigmentosum group A [Disease (Nov.)]
- xeroderma pigmentosum, group a [SNOMED Notion]
Has associated anatomic sites
- Integumentary System [NCIt concept]
See also inter- (CISMeF)
- XPA, DNA damage recognition and repair factor [ORDO Gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- XPA, DNA damage recognition and repair factor [ORDO Gene]
- Xeroderma pigmentosum, complementation group a [OMIM Phenotype]
- Xeroderma pigmentosum, group A (disorder) [SNOMED CT concept]
- xeroderma pigmentosum group A [Disease (Nov.)]
- xeroderma pigmentosum, group a [SNOMED Notion]
associated_with_malfunction_of_gene_product
- DNA Repair Protein Complementing XP-A Cells [NCIt concept]
- TFIIH Basal Transcription Factor Complex Helicase XPB Subunit [NCIt concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_has_associated_gene
- XPA Gene [NCIt concept]
- XPA wt Allele [NCIt concept]
disease_has_finding
- Cutaneous Involvement [NCIt concept]
disease_has_primary_anatomic_site
- Skin [NCIt concept]
disease_mapped_to_gene
- XPA Gene [NCIt concept]
disease_may_have_associated_disease
- Cutaneous Melanoma [NCIt concept]
- Skin Basal Cell Carcinoma [NCIt concept]
- Skin Squamous Cell Carcinoma [NCIt concept]
related_to_genetic_biomarker
- XPA Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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