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Phenotypic Abnormality (PA): Sensorineural hearing impairment

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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 ear [HP:0000598] <2>(17|32) (21|13|11)
+ + + 3:   Abnormal ear physiology [HP:0031704] <2>(7|10) (9|4|7)
+ + + 3:   Abnormal ear morphology [HP:0031703] <5>(15|26) (18|11|10)
+ + 2:   Hearing abnormality [HP:0000364] <3>(7|10) (9|4|7)
+ + 2:   Abnormality of the inner ear [HP:0000359] <5>(6|9) (8|4|3)
+ 1:   Functional abnormality of the inner ear [HP:0011389] <2>(6|6) (7|4|3)
+ 1:   Hearing impairment [HP:0000365] <13>(7|10) (9|4|7)
0:   Sensorineural hearing impairment [HP:0000407] <13>(4|3) (5|1|1)
- 1:   Childhood onset sensorineural hearing impairment [HP:0011474] <3>(0|0) (0|0|0)
- 1:   Adult onset sensorineural hearing impairment [HP:0008615](0|0) (0|0|0)
- 1:   Bilateral sensorineural hearing impairment [HP:0008619](1|1) (1|0|0)
- 1:   Congenital sensorineural hearing impairment [HP:0008527](1|1) (1|0|0)
- 1:   High-frequency sensorineural hearing impairment [HP:0001757](0|0) (0|0|0)
- 1:   Low-frequency sensorineural hearing impairment [HP:0008573](0|0) (0|0|0)
- 1:   Mild neurosensory hearing impairment [HP:0008587](0|0) (0|0|0)
- 1:   Mixed hearing impairment [HP:0000410](0|0) (0|0|0)
- 1:   Moderate sensorineural hearing impairment [HP:0008504](0|0) (1|0|0)
- 1:   Old-aged sensorineural hearing impairment [HP:0040113](0|0) (0|0|0)
- 1:   Profound sensorineural hearing impairment [HP:0011476](0|0) (0|0|0)
- 1:   Progressive sensorineural hearing impairment [HP:0000408](0|0) (0|0|0)
- 1:   Severe sensorineural hearing impairment [HP:0008625](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
ADC-like0Direct
Smc hinge domain0Direct
Integrin domains0.2397Inherited
Family A G protein-coupled receptor-like0.5646Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Smc hinge domain0Direct
Integrin domains0.2164Inherited
Rhodopsin-like0.4169Inherited


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)
Smc hinge domain0Direct
ADC-like0Direct
Integrin domains0.2038Inherited
Family A G protein-coupled receptor-like0.5212Inherited
Cysteine proteinases0.5968Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
103575,48726
  • 103575 - Plexin repeat
  • 48726 - Immunoglobulin
  • 0Direct

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    101912,103575,48726
  • 101912 - Sema domain
  • 103575 - Plexin repeat
  • 48726 - Immunoglobulin
  • 0Direct


    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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