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Phenotypic Abnormality (PA): Abnormality of the elbow

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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>(88|98) (93|55|34)
+ + + 3:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + 3:   Abnormality of limbs [HP:0040064] <8>(58|66) (63|33|25)
+ + 2:   Abnormality of the upper limb [HP:0002817] <20>(29|35) (35|17|16)
+ + 2:   Abnormal joint morphology [HP:0001367] <18>(19|23) (20|9|2)
+ 1:   Abnormality of upper limb joint [HP:0009810] <4>(4|5) (4|4|2)
0:   Abnormality of the elbow [HP:0009811] <17>(2|3) (2|2|2)
- 1:   Abnormality of the epiphyses of the elbow [HP:0003946] <5>(0|0) (0|0|0)
- 1:   Limited elbow movement [HP:0002996] <4>(1|1) (1|1|0)
- 1:   Abnormality of the elbow metaphyses [HP:0003949] <3>(0|0) (0|0|0)
- 1:   Abnormality of the humeroradial joint [HP:0100744] <2>(0|0) (0|0|0)
- 1:   Elbow dislocation [HP:0003042] <2>(1|2) (1|0|0)
- 1:   Synostosis involving the elbow [HP:0003938] <2>(0|0) (0|0|0)
- 1:   Abnormality of the humeroulnar joint [HP:0100745] <1>(0|0) (0|0|0)
- 1:   Abnormality of the joint spaces of the elbow [HP:0003943] <1>(0|0) (0|0|0)
- 1:   Cubitus valgus [HP:0002967](0|0) (0|0|0)
- 1:   Cubitus varus [HP:0025317](0|0) (0|0|0)
- 1:   Elbow ankylosis [HP:0003070](0|0) (0|1|1)
- 1:   Increased carrying angle [HP:0003102](0|0) (0|0|0)
- 1:   Irregular articular surfaces of the elbow joints [HP:0003945](0|0) (0|0|0)
- 1:   Large elbow [HP:0030865](0|0) (0|0|0)
- 1:   Osteoarthritis of the elbow [HP:0003940](0|0) (0|0|0)
- 1:   Stippled calcification of the elbow [HP:0003941](0|0) (0|0|0)
- 1:   Synovial chondromatosis of the elbow [HP:0003942](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Tropomyosin0.004586Inherited
ARID-like0.1728Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Exostosin0Direct
Tropomyosin0.003007Inherited
ARID domain0.1429Inherited


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)
Tropomyosin0.002768Inherited
ARID-like0.1424Inherited

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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
  • 0.000313Direct
    48726,48726
  • 48726 - Immunoglobulin
  • 48726 - Immunoglobulin
  • 0.2155Inherited

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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
  • 0.00007395Direct
    48726,48726,48726
  • 48726 - Immunoglobulin
  • 48726 - Immunoglobulin
  • 48726 - Immunoglobulin
  • 0.288Inherited


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
    (show help)