SUPERFAMILY 1.75 HMM library and genome assignments server

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Phenotypic Abnormality (PA): Hyposmia

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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 head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + 4:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + 3:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + 2:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
+ + 2:   Abnormality of the nose [HP:0000366] <19>(12|16) (15|7|3)
+ 1:   Abnormality of the sense of smell [HP:0004408] <2>(1|2) (3|2|0)
0:   Hyposmia [HP:0004409] <2>(0|0) (1|1|0)
- 1:   Partial hyposmia [HP:0010635](0|0) (0|0|0)
- 1:   Total hyposmia [HP:0010634](0|0) (0|0|0)


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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
(Phosphotyrosine protein) phosphatases II0.0007826Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
48371,48371
  • 48371 - ARM repeat
  • 48371 - ARM repeat
  • 0.00007366Direct


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