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Phenotypic Abnormality (PA): Short philtrum

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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)
+ + + + + + + + + + 10:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + + + + 9:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + + + + 8:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + + + + 7:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + + + + + 6:   Abnormality of the mouth [HP:0000153] <2>(37|57) (46|32|22)
+ + + + + 5:   Abnormal oral morphology [HP:0031816] <6>(35|53) (44|30|21)
+ + + + 4:   Abnormal oral cavity morphology [HP:0000163] <14>(28|43) (36|21|15)
+ + + 3:   Abnormal lip morphology [HP:0000159] <16>(5|9) (7|3|3)
+ + 2:   Abnormality of upper lip [HP:0000177] <7>(4|6) (5|2|3)
+ 1:   Abnormality of the philtrum [HP:0000288] <11>(2|4) (2|1|3)
0:   Short philtrum [HP:0000322](0|1) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Clathrin coat assembly domain0.0003626Direct


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