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Phenotypic Abnormality (PA): Delayed 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|54|34)
+ + + + 4:   Abnormal bone structure [HP:0003330] <12>(4|3) (5|2|4)
+ + + + 4:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + 3:   Abnormal bone ossification [HP:0011849] <5>(4|2) (4|0|2)
+ + + 3:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|42) (39|23|23)
+ + 2:   Abnormal enchondral ossification [HP:0003336] <12>(2|0) (2|0|0)
+ + 2:   Abnormality of long bone morphology [HP:0011314] <18>(6|10) (6|3|1)
+ 1:   Abnormal epiphyseal ossification [HP:0010656] <7>(1|0) (1|0|0)
+ 1:   Abnormality of epiphysis morphology [HP:0005930] <21>(3|2) (3|0|0)
0:   Delayed epiphyseal ossification [HP:0002663] <3>(1|0) (1|0|0)
- 1:   Delayed upper limb epiphyseal ossification [HP:0003840] <2>(0|0) (0|0|0)
- 1:   Delayed phalangeal epiphyseal ossification [HP:0006016](0|0) (0|0|0)
- 1:   Delayed proximal femoral epiphyseal ossification [HP:0008828](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Cytochrome P4500.00005472Direct


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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 P4500.00002467Direct


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