Xeroderma pigmentosum group A
Xeroderma pigmentosum group A
Definition
Any xeroderma pigmentosum in which the cause of the disease is a mutation in the XPA gene.
Also known as xeroderma pigmentosum 1, xeroderma pigmentosum caused by mutation in XPA, xeroderma pigmentosum group A, xeroderma pigmentosum group type A, xeroderma pigmentosum, complementation group type a, xeroderma pigmentosum, group A, XP-A, XP1, XPA, XPA xeroderma pigmentosum — per MONDO
Also identified as
- DOID 0110843 per MONDO
- NCIT C3965 per MONDO
- OMIM 278700 per MONDO
- Orphanet 276249 per MONDO
- SCTID 43477006 per MONDO
- UMLS C0268135 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Integumental system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Skin of body | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |