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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
xeroderma pigmentosum +     
De Sanctis-Cacchione syndrome  
photosensitive trichothiodystrophy 1  
xeroderma pigmentosum group A  
xeroderma pigmentosum group B  
xeroderma pigmentosum group C  
xeroderma pigmentosum group D  
A xeroderma pigmentosum that has_material_basis_in homozygous or compound heterozygous mutation in the excision repair gene ERCC2 on chromosome 19q13. (DO)
xeroderma pigmentosum group E  
xeroderma pigmentosum group F  
xeroderma pigmentosum group G  
xeroderma pigmentosum variant type  
Xeroderma Pigmentosum, Autosomal Dominant, Mild 
Xeroderma Pigmentosum, Type 9 
XFE progeroid syndrome  

Synonyms
Exact Synonyms: XP, Group D ;   XP, group H ;   XP4 ;   XP4 XERODERMA PIGMENTOSUM VIII ;   XP8 ;   XPD ;   XPDC ;   XPH ;   xeroderma pigmentosum IV ;   xeroderma pigmentosum VIII
Primary IDs: MESH:C562591
Alternate IDs: MIM:278730 ;   RDO:0012239
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/7849702 "DO" "DO"

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