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Phenotypic Abnormality (PA): Spina bifida occulta at S1

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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)
+ + + + + + + + 8:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + + 7:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + + + 6:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ + + + + 5:   Abnormal neural tube morphology [HP:0410043] <1>(3|5) (3|0|0)
+ + + + + 5:   Morphological abnormality of the central nervous system [HP:0002011] <17>(60|85) (69|44|16)
+ + + + 4:   Neural tube defect [HP:0045005] <3>(3|5) (3|0|0)
+ + + + 4:   Abnormality of the spinal cord [HP:0002143] <16>(3|5) (3|0|2)
+ + + 3:   Spinal dysraphism [HP:0010301] <1>(3|5) (3|0|0)
+ + 2:   Spina bifida [HP:0002414] <3>(2|4) (2|0|0)
+ 1:   Spina bifida occulta [HP:0003298] <2>(2|3) (2|0|0)
0:   Spina bifida occulta at S1 [HP:0004614](0|0) (0|0|0)