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Phenotypic Abnormality (PA): Abnormality of finger

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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:   Abnormality of skeletal morphology [HP:0011842] <19>(82|83) (88|48|29)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the skeletal system [HP:0000924] <7>(87|94) (95|55|32)
+ + + 3:   Abnormality of limb bone [HP:0040068] <1>(25|27) (27|18|18)
+ + + 3:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(33|39) (37|23|21)
+ + + 3:   Abnormality of limbs [HP:0040064] <8>(55|63) (58|31|22)
+ + 2:   Abnormality of the upper limb [HP:0002817] <20>(26|31) (31|19|15)
+ + 2:   Abnormality of limb bone morphology [HP:0002813] <13>(25|27) (27|18|18)
+ 1:   Abnormal digit morphology [HP:0011297] <10>(18|20) (18|16|16)
+ 1:   Abnormality of the hand [HP:0001155] <26>(20|26) (25|17|13)
0:   Abnormality of finger [HP:0001167] <24>(11|16) (13|12|10)
- 1:   Abnormal finger phalanx morphology [HP:0005918] <24>(7|8) (8|6|3)
- 1:   Aplasia/Hypoplasia of fingers [HP:0006265] <9>(1|4) (1|2|4)
- 1:   Deviation of finger [HP:0004097] <9>(1|2) (1|0|0)
- 1:   Abnormal 5th finger morphology [HP:0004207] <8>(3|2) (3|0|0)
- 1:   Abnormal thumb morphology [HP:0001172] <8>(1|5) (4|7|7)
- 1:   Abnormal 2nd finger morphology [HP:0004100] <6>(1|2) (1|0|0)
- 1:   Abnormal 3rd finger morphology [HP:0004150] <6>(0|0) (0|0|0)
- 1:   Abnormal 4th finger morphology [HP:0004188] <6>(0|0) (0|0|0)
- 1:   Curved fingers [HP:0004095] <5>(0|0) (0|0|0)
- 1:   Abnormal fingertip morphology [HP:0001211] <3>(0|0) (0|0|0)
- 1:   Abnormal finger flexion creases [HP:0006143] <2>(0|0) (0|0|0)
- 1:   Finger joint hypermobility [HP:0006094] <2>(1|1) (1|1|0)
- 1:   Long fingers [HP:0100807] <2>(0|1) (0|1|0)
- 1:   Broad finger [HP:0001500] <1>(0|0) (0|0|0)
- 1:   Slender finger [HP:0001238] <1>(0|1) (1|2|0)
- 1:   Chilblains [HP:0009710](0|0) (0|0|0)
- 1:   Finger dactylitis [HP:0031090](0|0) (0|0|0)
- 1:   Finger swelling [HP:0025131](1|1) (1|0|0)
- 1:   Macrodactyly of finger [HP:0100746](0|0) (0|0|0)
- 1:   Mallet finger [HP:0030771](0|0) (0|0|0)
- 1:   Spindle-shaped finger [HP:0031092](0|0) (0|0|0)
- 1:   Splayed fingers [HP:0030029](0|0) (0|0|0)
- 1:   Swan neck-like deformities of the fingers [HP:0006150](0|0) (0|0|0)
- 1:   Trident hand [HP:0004060](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
RuvA domain 2-like0Direct
BRK domain-like0Direct
ARID-like0.01325Inherited
Restriction endonuclease-like0.01339Inherited
Insulin-like0.01339Inherited
WD40 repeat-like0.06686Inherited
HLH, helix-loop-helix DNA-binding domain0.07842Inherited
Cystine-knot cytokines0.1881Inherited
GroEL equatorial domain-like0.3878Inherited
N-terminal nucleophile aminohydrolases (Ntn hydrolases)0.3878Inherited
vWA-like0.6748Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
XPF/Rad1/Mus81 nuclease0Direct
BRK domain-like0Direct
Proteasome subunits0Direct
Erythroid transcription factor GATA-10.0001423Direct
Actin/HSP700.0007577Direct
ARID domain0.0089Inherited
Insulin-like0.008995Inherited
RecA protein-like (ATPase-domain)0.06008Inherited
HLH, helix-loop-helix DNA-binding domain0.0616Inherited
Transforming growth factor (TGF)-beta0.07392Inherited
Classic zinc finger, C2H20.1012Inherited
VWC domain0.2708Inherited
Sema domain0.2708Inherited
Homeodomain0.3445Inherited
Integrin A (or I) domain0.5555Inherited
TB module/8-cys domain0.6194Inherited


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)
RuvA domain 2-like0Direct
BRK domain-like0Direct
ARID-like0.008828Inherited
Insulin-like0.008925Inherited
Restriction endonuclease-like0.008925Inherited
WD40 repeat-like0.05115Inherited
HLH, helix-loop-helix DNA-binding domain0.06081Inherited
Cystine-knot cytokines0.1572Inherited
Sema domain0.2659Inherited
GroEL equatorial domain-like0.3466Inherited
N-terminal nucleophile aminohydrolases (Ntn hydrolases)0.3466Inherited
TB module/8-cys domain0.6105Inherited
vWA-like0.6356Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
52980,47781
  • 52980 - Restriction endonuclease-like
  • 47781 - RuvA domain 2-like
  • 0Direct
    103575,48726
  • 103575 - Plexin repeat
  • 48726 - Immunoglobulin
  • 0.008925Inherited
    53300,53300
  • 53300 - vWA-like
  • 53300 - vWA-like
  • 0.02689Inherited
    50729,50729
  • 50729 - PH domain-like
  • 50729 - PH domain-like
  • 0.02689Inherited
    57196,57184
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.0932Inherited
    57667,57667
  • 57667 - beta-beta-alpha zinc fingers
  • 57667 - beta-beta-alpha zinc fingers
  • 0.2008Inherited
    101912,103575
  • 101912 - Sema domain
  • 103575 - Plexin repeat
  • 0.2659Inherited
    81296,81296
  • 81296 - E set domains
  • 81296 - E set domains
  • 0.3466Inherited
    57903,57903
  • 57903 - FYVE/PHD zinc finger
  • 57903 - FYVE/PHD zinc finger
  • 0.3466Inherited
    57184,57184
  • 57184 - Growth factor receptor domain
  • 57184 - Growth factor receptor domain
  • 0.5459Inherited
    57581,57196
  • 57581 - TB module/8-cys domain
  • 57196 - EGF/Laminin
  • 0.6105Inherited
    57196,57581
  • 57196 - EGF/Laminin
  • 57581 - TB module/8-cys domain
  • 0.6105Inherited

    (show details)
    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57184,57184,57196
  • 57184 - Growth factor receptor domain
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 0Direct
    57196,57581,57196
  • 57196 - EGF/Laminin
  • 57581 - TB module/8-cys domain
  • 57196 - EGF/Laminin
  • 0Direct
    57196,57196,57581
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57581 - TB module/8-cys domain
  • 0Direct
    57196,57581,57184
  • 57196 - EGF/Laminin
  • 57581 - TB module/8-cys domain
  • 57184 - Growth factor receptor domain
  • 0Direct
    101912,103575,48726
  • 101912 - Sema domain
  • 103575 - Plexin repeat
  • 48726 - Immunoglobulin
  • 0.008925Inherited
    57196,57196,57184
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.122Inherited
    57196,57184,57184
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 57184 - Growth factor receptor domain
  • 0.1582Inherited
    81296,81296,81296
  • 81296 - E set domains
  • 81296 - E set domains
  • 81296 - E set domains
  • 0.3466Inherited
    57581,57196,57196
  • 57581 - TB module/8-cys domain
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.6105Inherited
    57581,57196,57581
  • 57581 - TB module/8-cys domain
  • 57196 - EGF/Laminin
  • 57581 - TB module/8-cys domain
  • 0.6105Inherited


    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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