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Phenotypic Abnormality (PA): Aplasia/Hypoplasia involving bones of the feet

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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:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + + + + 5:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + + 4:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|42) (39|23|23)
+ + + + 4:   Aplasia/hypoplasia involving the skeleton [HP:0009115] <2>(13|11) (15|10|17)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of limb bone [HP:0040068] <1>(29|31) (33|18|20)
+ + + 3:   Abnormality of limbs [HP:0040064] <8>(58|65) (63|33|25)
+ + + 3:   Aplasia/hypoplasia of the extremities [HP:0009815] <6>(8|9) (10|3|5)
+ + + 3:   Abnormality of limb bone morphology [HP:0002813] <13>(29|31) (32|18|20)
+ + 2:   Abnormal lower limb bone morphology [HP:0040069] <10>(11|9) (12|5|6)
+ + 2:   Aplasia/hypoplasia involving bones of the extremities [HP:0045060] <3>(7|8) (9|3|5)
+ + 2:   Abnormality of the lower limb [HP:0002814] <17>(31|34) (35|15|13)
+ 1:   Abnormality of the foot [HP:0001760] <30>(20|24) (21|13|10)
+ 1:   Aplasia/hypoplasia involving bones of the lower limbs [HP:0006493] <10>(5|5) (6|3|4)
0:   Aplasia/Hypoplasia involving bones of the feet [HP:0006494] <8>(4|4) (5|2|3)
- 1:   Aplasia/Hypoplasia of the phalanges of the toes [HP:0010173] <10>(2|2) (2|0|0)
- 1:   Aplasia/Hypoplasia of metatarsal bones [HP:0001964] <3>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of toe [HP:0001991] <3>(3|3) (4|2|2)
- 1:   Aplasia/Hypoplasia of the tarsal bones [HP:0008363] <2>(0|0) (0|0|0)
- 1:   Absent foot [HP:0011301](0|0) (0|0|0)
- 1:   Lower limb peromelia [HP:0009820](0|0) (0|0|0)
- 1:   Partial absence of foot [HP:0030032](0|0) (0|0|0)
- 1:   Short foot [HP:0001773](1|1) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
ARID-like0.00007631Direct
Arginase/deacetylase0.000215Direct
HMG-box0.01112Inherited
Immunoglobulin0.7934Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Histone deacetylase, HDAC0Direct
ARID domain0.0000395Direct
HMG-box0.007747Inherited
I set domains0.3143Inherited


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-like0.0000348Direct
Arginase/deacetylase0.0001039Direct
HMG-box0.007194Inherited
Cystine-knot cytokines0.1446Inherited
Immunoglobulin0.758Inherited

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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
  • 0.01108Inherited
    48726,48726
  • 48726 - Immunoglobulin
  • 48726 - Immunoglobulin
  • 0.5242Inherited

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    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
  • 0.0001039Direct
    57196,57196,57184
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.003023Inherited
    48726,48726,48726
  • 48726 - Immunoglobulin
  • 48726 - Immunoglobulin
  • 48726 - Immunoglobulin
  • 0.4394Inherited


    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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