has material basis in germline mutation in
XPA
xeroderma pigmentosum group A
https://github.com/monarch-initiative/mondo/issues/4521
Orphanet:276249
xeroderma pigmentosum group type A
xeroderma pigmentosum caused by mutation in XPA
xeroderma pigmentosum, group A
XP group A
MONDO:0010210
XP1
xeroderma pigmentosum complementation group A
XPA xeroderma pigmentosum
SCTID:43477006
XP-A
xeroderma pigmentosum, complementation group type a
XPA
xeroderma pigmentosum 1
OMIM:278700
GARD:5624
xeroderma pigmentosum, complementation group A
xeroderma pigmentosum group A
Any xeroderma pigmentosum in which the cause of the disease is a mutation in the XPA gene.
DOID:0110843
UMLS:C0268135
NCIT:C3965
xeroderma pigmentosum, type 1
XP, group A
xeroderma pigmentosum