Disease #00747 (XPD (xeroderma pigmentosum, complementation group D (XPD)), OMIM:278730)

Official abbreviation XPD
Name xeroderma pigmentosum, complementation group D (XPD)
OMIM ID 278730
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene ERCC2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00436177 XP14KA.1 PubMed: Ben Rekaya 2018 4-generation family, 3 affected, sister unaffected heterozygous parents/relatives F - Tunisia - - - - - XPD see paper; ... - CERS3, ERCC2 2 3 Johan den Dunnen
00436178 XP25K PubMed: Ben Rekaya 2018 5-generation family, 4 affected (F, 3M), unaffected heterozygous parents/relatives F;M yes Tunisia - - - - - XPD see paper; ... - ERCC2 1 4 Johan den Dunnen
00436179 XP125KA PubMed: Ben Rekaya 2018 4-generation family, 3 affected sisters, unaffected heterozygous parents/relatives F yes Tunisia - - - - - XPD see paper; ... - ERCC2 1 3 Johan den Dunnen
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