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Phenotypic Abnormality (PA): Absent toe

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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)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Abnormality of skeletal morphology [HP:0011842] <18>(87|89) (90|49|32)
+ + + + + + 6:   Aplasia/hypoplasia involving the skeleton [HP:0009115] <2>(13|11) (13|10|17)
+ + + + + + 6:   Abnormality of the skeletal system [HP:0000924] <7>(89|98) (94|51|33)
+ + + + + 5:   Aplasia/hypoplasia of the extremities [HP:0009815] <6>(8|9) (9|3|5)
+ + + + + 5:   Abnormality of limb bone [HP:0040068] <1>(28|30) (30|18|20)
+ + + + + 5:   Abnormality of limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + + + + 5:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|41) (38|23|23)
+ + + + 4:   Abnormality of the lower limb [HP:0002814] <17>(30|31) (33|14|13)
+ + + + 4:   Aplasia/hypoplasia involving bones of the extremities [HP:0045060] <3>(7|8) (8|3|5)
+ + + + 4:   Abnormality of limb bone morphology [HP:0002813] <13>(28|30) (30|18|20)
+ + + + 4:   Abnormal lower limb bone morphology [HP:0040069] <10>(10|8) (11|5|6)
+ + + 3:   Abnormality of the foot [HP:0001760] <30>(19|21) (19|12|10)
+ + + 3:   Abnormal digit morphology [HP:0011297] <10>(16|19) (17|14|16)
+ + + 3:   Aplasia/hypoplasia involving bones of the lower limbs [HP:0006493] <10>(5|4) (5|3|4)
+ + 2:   Aplasia/Hypoplasia involving bones of the feet [HP:0006494] <8>(4|3) (4|2|3)
+ + 2:   Abnormality of toe [HP:0001780] <27>(7|6) (7|4|2)
+ 1:   Aplasia/Hypoplasia of toe [HP:0001991] <3>(3|2) (3|2|2)
0:   Absent toe [HP:0010760] <9>(2|1) (2|1|1)
- 1:   Aplasia/Hypoplasia of the distal phalanges of the toes [HP:0010185] <7>(1|1) (1|0|0)
- 1:   Aplasia/Hypoplasia of the 2nd toe [HP:0010325] <5>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the 3rd toe [HP:0010331] <5>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the 4th toe [HP:0010337] <5>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the 5th toe [HP:0010343] <5>(1|1) (1|0|0)
- 1:   Aplasia/Hypoplasia of the hallux [HP:0008362] <3>(1|0) (1|0|0)
- 1:   Adactyly [HP:0009776] <1>(0|0) (0|0|0)
- 1:   Foot oligodactyly [HP:0001849] <1>(0|0) (0|0|0)
- 1:   Partial absence of toe [HP:0011305](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
ARID-like0.00002091Direct
Cystine-knot cytokines0.007736Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
ARID domain0.00001576Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
ARID-like0.000009483Direct
Cystine-knot cytokines0.004959Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57196,57184
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.0004359Direct

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57196,57196,57184
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.0001642Direct


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