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Phenotypic Abnormality (PA): Aplasia/Hypoplasia of 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)
+ + + + + 5:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ + + + + 5:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Aplasia/hypoplasia involving the skeleton [HP:0009115] <2>(13|12) (15|10|17)
+ + + + 4:   Abnormality of limb bone [HP:0040068] <1>(29|32) (33|18|20)
+ + + + 4:   Abnormality of limbs [HP:0040064] <8>(58|66) (63|33|25)
+ + + + 4:   Aplasia/hypoplasia of the extremities [HP:0009815] <6>(8|10) (10|3|5)
+ + + + 4:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|43) (39|23|23)
+ + + 3:   Aplasia/hypoplasia involving bones of the extremities [HP:0045060] <3>(7|9) (9|3|5)
+ + + 3:   Abnormality of limb bone morphology [HP:0002813] <13>(29|32) (32|18|20)
+ + + 3:   Abnormality of the lower limb [HP:0002814] <17>(31|34) (35|15|13)
+ + + 3:   Abnormal lower limb bone morphology [HP:0040069] <10>(11|9) (12|5|6)
+ + 2:   Abnormal digit morphology [HP:0011297] <10>(16|21) (18|14|16)
+ + 2:   Aplasia/hypoplasia involving bones of the lower limbs [HP:0006493] <10>(5|5) (6|3|4)
+ + 2:   Abnormality of the foot [HP:0001760] <30>(20|24) (21|13|10)
+ 1:   Abnormality of toe [HP:0001780] <27>(6|7) (8|4|2)
+ 1:   Aplasia/Hypoplasia involving bones of the feet [HP:0006494] <8>(4|4) (5|2|3)
0:   Aplasia/Hypoplasia of toe [HP:0001991] <3>(3|3) (4|2|2)
- 1:   Absent toe [HP:0010760] <9>(2|2) (3|1|1)
- 1:   Short toe [HP:0001831] <8>(1|1) (2|1|1)
- 1:   Small toe [HP:0030031](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
HMG-box0.004809Inherited
ARID-like0.01446Inherited
Immunoglobulin0.2232Inherited


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
HMG-box0.004947Inherited
ARID domain0.01357Inherited
I set domains0.05317Inherited


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)
HMG-box0.002914Inherited
ARID-like0.009578Inherited
Cystine-knot cytokines0.02857Inherited
Immunoglobulin0.1886Inherited

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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
  • 0.02857Inherited
    48726,48726
  • 48726 - Immunoglobulin
  • 48726 - Immunoglobulin
  • 0.07403Inherited

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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
  • 0.02857Inherited
    48726,48726,48726
  • 48726 - Immunoglobulin
  • 48726 - Immunoglobulin
  • 48726 - Immunoglobulin
  • 0.03945Inherited


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