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Ontology Browser

Term:
xeroderma pigmentosum group B (DOID:0110850)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
De Sanctis-Cacchione Syndrome  
photosensitive trichothiodystrophy 1  
xeroderma pigmentosum group A  
xeroderma pigmentosum group B +   
A xeroderma pigmentosum characterized by that has_material_basis_in mutation in the ERCC3 gene on chromosome 2q14. (DO)
xeroderma pigmentosum group C  
xeroderma pigmentosum group D  
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: XPB ;   XPBC ;   xeroderma pigmentosum, complementation group B
Narrow Synonyms: XP, GROUP B ;   XPB/CS ;   XPBC XERODERMA PIGMENTOSUM B/COCKAYNE SYNDROME
Primary IDs: MESH:C562590
Alternate IDs: OMIM:610651 ;   RDO:0012238
Xrefs: NCI:C3966
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/16947863 "DO"

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.