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Phenotypic Abnormality (PA): Abnormality of the knee

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the skeletal system [HP:0000924] <7>(89|98) (94|51|33)
+ + + 3:   Abnormality of limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + + 3:   Abnormality of skeletal morphology [HP:0011842] <18>(87|89) (90|49|32)
+ + 2:   Abnormal joint morphology [HP:0001367] <18>(18|22) (20|9|2)
+ + 2:   Abnormality of the lower limb [HP:0002814] <17>(30|31) (33|14|13)
+ 1:   Abnormality of lower limb joint [HP:0100491] <5>(10|12) (11|2|1)
0:   Abnormality of the knee [HP:0002815] <15>(3|4) (4|1|1)
- 1:   Abnormal patella morphology [HP:0003045] <10>(2|2) (2|0|0)
- 1:   Hyperextensibility of the knee [HP:0010500] <2>(0|0) (0|0|0)
- 1:   Abnormal meniscus morphology [HP:0032190] <1>(0|0) (0|0|0)
- 1:   Genu valgum [HP:0002857] <1>(0|0) (0|0|0)
- 1:   Genu varum [HP:0002970] <1>(0|0) (0|0|0)
- 1:   Knee dislocation [HP:0004976] <1>(0|0) (0|0|0)
- 1:   Limited knee extension [HP:0003066] <1>(0|0) (1|0|0)
- 1:   Limited knee flexion [HP:0006389] <1>(0|0) (0|0|0)
- 1:   Absent knee epiphyses [HP:0006400](0|0) (0|0|0)
- 1:   Flattened knee epiphyses [HP:0005715](0|0) (0|0|0)
- 1:   Knee flexion contracture [HP:0006380](1|1) (1|1|0)
- 1:   Knee osteoarthritis [HP:0005086](0|0) (0|0|0)
- 1:   Large knee [HP:0030866](0|0) (0|0|0)
- 1:   Limitation of knee mobility [HP:0010501](0|0) (0|0|0)
- 1:   Popliteal synovial cyst [HP:0032072](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
ARID-like0.003072Inherited
Tropomyosin0.2087Inherited
Bromodomain0.3012Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Filamin repeat (rod domain)0Direct
ARID domain0.002093Inherited
Tropomyosin0.1936Inherited
Bromodomain0.289Inherited


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)
ARID-like0.001815Inherited
Tropomyosin0.1759Inherited
Bromodomain0.2629Inherited
Voltage-gated potassium channels0.4601Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
53300,53300
  • 53300 - vWA-like
  • 53300 - vWA-like
  • 0.0007439Direct

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57184,57196,57184
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.0001838Direct


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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