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Phenotypic Abnormality (PA): Scleroderma

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the integument [HP:0001574] <4>(48|69) (59|37|15)
+ + + 3:   Abnormality of the skin [HP:0000951] <4>(34|55) (45|36|12)
+ + 2:   Abnormality of skin morphology [HP:0011121] <22>(29|49) (40|31|11)
+ 1:   Thickened skin [HP:0001072] <4>(3|6) (3|6|2)
0:   Scleroderma [HP:0100324] <1>(0|0) (0|0|0)
- 1:   Proximal scleroderma [HP:0550003](0|0) (0|0|0)