SUPERFAMILY 1.75 HMM library and genome assignments server

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Phenotypic Abnormality (PA): Mediastinal lymphadenopathy

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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)
+ + + + + 5:   Abnormality of the cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ + + + 4:   Abnormality of the immune system [HP:0002715] <3>(38|52) (40|29|16)
+ + + + 4:   Abnormality of the vasculature [HP:0002597] <13>(35|56) (45|27|18)
+ + + 3:   Abnormality of the lymphatic system [HP:0100763] <7>(9|19) (15|8|5)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the lymph nodes [HP:0002733] <6>(3|9) (7|5|2)
+ + 2:   Abnormality of the thoracic cavity [HP:0045027] <1>(0|0) (2|0|0)
+ 1:   Lymphadenopathy [HP:0002716] <5>(2|8) (6|5|2)
+ 1:   Abnormality of the mediastinum [HP:0045026] <2>(0|0) (1|0|0)
0:   Mediastinal lymphadenopathy [HP:0100721](0|0) (1|0|0)


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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
SH3-domain0.0009576Direct


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