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Disease Ontology (DO): xeroderma pigmentosum

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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Root: DO Hierarchy (disease ontology from University of Maryland)

Shortest distance to current term (+ for parents, - for children) DO term [DO ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   disease [DOID:4] <8>
+ + + + 4:   genetic disease [DOID:630] <11>(19|28) (22|16|7)
+ + + 3:   monogenic disease [DOID:0050177] <7>(17|25) (19|14|6)
+ + 2:   autosomal genetic disease [DOID:0050739] <8>(17|24) (19|14|6)
+ 1:   autosomal recessive disease [DOID:0050737] <89>(10|11) (10|6|3)
0:   xeroderma pigmentosum [DOID:0050427] <8>(0|0) (0|0|0)
- 1:   xeroderma pigmentosum group A [DOID:0110843](0|0) (0|0|0)
- 1:   xeroderma pigmentosum group B [DOID:0110850](0|0) (0|0|0)
- 1:   xeroderma pigmentosum group C [DOID:0110844](0|0) (0|0|0)
- 1:   xeroderma pigmentosum group D [DOID:0110845](0|0) (0|0|0)
- 1:   xeroderma pigmentosum group E [DOID:0110846](0|0) (0|0|0)
- 1:   xeroderma pigmentosum group F [DOID:0110848](0|0) (0|0|0)
- 1:   xeroderma pigmentosum group G [DOID:0110849](0|0) (0|0|0)
- 1:   xeroderma pigmentosum variant type [DOID:0110847](0|0) (0|0|0)