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Phenotypic Abnormality (PA): Aplasia/hypoplasia involving bones of the upper limbs

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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 the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + + + 4:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + 3:   Abnormality of limb bone [HP:0040068] <1>(29|31) (33|18|20)
+ + + 3:   Aplasia/hypoplasia involving the skeleton [HP:0009115] <2>(13|11) (15|10|17)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|42) (39|23|23)
+ + 2:   Abnormality of limbs [HP:0040064] <8>(58|65) (63|33|25)
+ + 2:   Aplasia/hypoplasia of the extremities [HP:0009815] <6>(8|9) (10|3|5)
+ + 2:   Abnormality of limb bone morphology [HP:0002813] <13>(29|31) (32|18|20)
+ 1:   Abnormality of the upper limb [HP:0002817] <20>(29|34) (35|17|16)
+ 1:   Aplasia/hypoplasia involving bones of the extremities [HP:0045060] <3>(7|8) (9|3|5)
0:   Aplasia/hypoplasia involving bones of the upper limbs [HP:0006496] <8>(3|7) (6|2|4)
- 1:   Aplasia/hypoplasia involving bones of the hand [HP:0005927] <6>(3|5) (6|2|4)
- 1:   Aplasia/hypoplasia involving forearm bones [HP:0006503] <5>(0|1) (0|0|0)
- 1:   Aplasia/hypoplasia of the humerus [HP:0006507] <3>(0|0) (0|0|0)
- 1:   Aplasia involving bones of the upper limbs [HP:0009823] <1>(0|1) (0|0|0)
- 1:   Upper limb undergrowth [HP:0009824] <1>(0|1) (0|0|0)
- 1:   Amelia involving the upper limbs [HP:0009812](0|0) (0|0|0)
- 1:   Upper limb peromelia [HP:0009814](0|0) (0|0|0)
- 1:   Upper limb phocomelia [HP:0009813](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
ARID-like0.001216Inherited
Multidrug efflux transporter AcrB transmembrane domain0.006228Inherited
p53-like transcription factors0.2199Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Histone deacetylase, HDAC0Direct
ARID domain0.0006896Direct
Notch domain0.001114Inherited
BRK domain-like0.001114Inherited
RecA protein-like (ATPase-domain)0.02533Inherited
Transforming growth factor (TGF)-beta0.3872Inherited
I set domains0.5202Inherited


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-like0.0006536Direct
Arginase/deacetylase0.001075Inherited
Notch domain0.001075Inherited
BRK domain-like0.001075Inherited
Multidrug efflux transporter AcrB transmembrane domain0.003861Inherited
p53-like transcription factors0.1856Inherited

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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
  • 0.04Inherited
    81296,81296
  • 81296 - E set domains
  • 81296 - E set domains
  • 0.1263Inherited

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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
  • 0Direct
    57196,57196,57184
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.01716Inherited
    57196,57184,57184
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 57184 - Growth factor receptor domain
  • 0.03422Inherited
    81296,81296,81296
  • 81296 - E set domains
  • 81296 - E set domains
  • 81296 - E set domains
  • 0.1263Inherited


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