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Phenotypic Abnormality (PA): Malabsorption

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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:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the digestive system [HP:0025031] <6>(63|72) (76|45|24)
+ + + 3:   Abnormality of the gastrointestinal tract [HP:0011024] <3>(22|26) (28|11|3)
+ + + 3:   Abnormality of digestive system morphology [HP:0025033] <2>(12|18) (17|6|3)
+ + 2:   Morphological abnormality of the gastrointestinal tract [HP:0012718] <8>(12|18) (17|6|3)
+ 1:   Abnormal intestine morphology [HP:0002242] <22>(9|11) (13|3|0)
0:   Malabsorption [HP:0002024] <2>(2|2) (2|1|0)
- 1:   Fat malabsorption [HP:0002630] <1>(1|0) (1|0|0)
- 1:   Lactose intolerance [HP:0004789](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase0.0009776Direct
alpha/beta-Hydrolases0.05004Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
DNA gyrase/MutL, second domain0.000004631Direct
DNA gyrase/MutL, N-terminal domain0.000004631Direct


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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)
ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase0.0005324Direct
alpha/beta-Hydrolases0.03728Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
55874,54211
  • 55874 - ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase
  • 54211 - Ribosomal protein S5 domain 2-like
  • 0.000003624Direct


    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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