SUPERFAMILY 1.75 HMM library and genome assignments server

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Phenotypic Abnormality (PA): Amyloidosis

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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)
+ + 2:   Phenotypic abnormality [HP:0000118] <25>
+ 1:   Abnormality of metabolism/homeostasis [HP:0001939] <16>(75|82) (79|40|16)
0:   Amyloidosis [HP:0011034] <8>(1|1) (1|0|0)
- 1:   Cutaneous amyloidosis [HP:0012309] <3>(0|0) (0|0|0)
- 1:   Cardiac amyloidosis [HP:0030843] <2>(0|0) (0|0|0)
- 1:   Amyloidosis of peripheral nerves [HP:0100292](0|0) (0|0|0)
- 1:   Cerebral amyloid angiopathy [HP:0011970](0|0) (0|0|0)
- 1:   Conjunctival amyloidosis [HP:0010637](0|0) (0|0|0)
- 1:   Generalized amyloid deposition [HP:0003216](0|0) (0|0|0)
- 1:   Hepatic amyloidosis [HP:0012280](0|0) (0|0|0)
- 1:   Renal amyloidosis [HP:0001917](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
DEATH domain0.000282Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Pyrin domain, PYD0.0000006737Direct


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)
DEATH domain0.0001383Direct


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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