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Phenotypic Abnormality (PA): Abnormal epiphyseal ossification

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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)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ + + + 4:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + 3:   Abnormal bone structure [HP:0003330] <12>(4|3) (5|2|4)
+ + 2:   Abnormal bone ossification [HP:0011849] <5>(4|2) (4|0|2)
+ 1:   Abnormal enchondral ossification [HP:0003336] <12>(2|0) (2|0|0)
0:   Abnormal epiphyseal ossification [HP:0010656] <7>(1|0) (1|0|0)
- 1:   Epiphyseal stippling [HP:0010655] <7>(0|0) (0|0|0)
- 1:   Delayed epiphyseal ossification [HP:0002663] <3>(1|0) (1|0|0)
- 1:   Irregular ossification of the humeral epiphyses [HP:0003897] <2>(0|0) (0|0|0)
- 1:   Absent ossification of capital femoral epiphysis [HP:0008820](0|0) (0|0|0)
- 1:   Advanced ossification of the humeral epiphysis [HP:0003893](0|0) (0|0|0)
- 1:   Early ossification of capital femoral epiphyses [HP:0008797](0|0) (0|0|0)
- 1:   Premature fusion of phalangeal epiphyses [HP:0006140](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Cytochrome P4500.002148Inherited


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

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Cytochrome P4500.001211Inherited


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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