SUPERFAMILY 1.75 HMM library and genome assignments server

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Phenotypic Abnormality (PA): Type I diabetes mellitus

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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 metabolism/homeostasis [HP:0001939] <16>(75|82) (79|40|16)
+ + + + 4:   Abnormal homeostasis [HP:0012337] <8>(44|47) (44|22|8)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormal glucose homeostasis [HP:0011014] <7>(11|12) (12|7|4)
+ + 2:   Abnormality of the endocrine system [HP:0000818] <16>(28|35) (35|13|5)
+ + 2:   Glucose intolerance [HP:0001952] <2>(4|4) (5|3|3)
+ 1:   Diabetes mellitus [HP:0000819] <6>(3|3) (4|2|3)
0:   Type I diabetes mellitus [HP:0100651](1|1) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Trypsin-like serine proteases0.0008692Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Eukaryotic proteases0.000383Direct


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)
Trypsin-like serine proteases0.0004553Direct


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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