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Phenotypic Abnormality (PA): Epiphyseal dysplasia

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|42) (39|23|23)
+ + + 3:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + 2:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + 2:   Abnormality of long bone morphology [HP:0011314] <18>(6|10) (6|3|1)
+ 1:   Skeletal dysplasia [HP:0002652] <9>(1|0) (2|0|0)
+ 1:   Abnormality of epiphysis morphology [HP:0005930] <21>(3|2) (3|0|0)
0:   Epiphyseal dysplasia [HP:0002656](1|0) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Concanavalin A-like lectins/glucanases0.0008756Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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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)
Concanavalin A-like lectins/glucanases0.0004599Direct


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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