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Phenotypic Abnormality (PA): Abnormality of the fascia

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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)
+ + 2:   Phenotypic abnormality [HP:0000118] <25>
+ 1:   Abnormality of connective tissue [HP:0003549] <12>(19|27) (19|20|20)
0:   Abnormality of the fascia [HP:0100536] <1>(0|0) (0|0|0)
- 1:   Fasciitis [HP:0100537] <1>(0|0) (0|0|0)