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Phenotypic Abnormality (PA): Aplasia/Hypoplasia of fingers

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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>(89|98) (94|51|33)
+ + + + + 5:   Aplasia/hypoplasia involving the skeleton [HP:0009115] <2>(13|11) (13|10|17)
+ + + + + 5:   Abnormality of skeletal morphology [HP:0011842] <18>(87|89) (90|49|32)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Aplasia/hypoplasia of the extremities [HP:0009815] <6>(8|9) (9|3|5)
+ + + + 4:   Abnormality of limb bone [HP:0040068] <1>(28|30) (30|18|20)
+ + + + 4:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|41) (38|23|23)
+ + + + 4:   Abnormality of limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + + 3:   Abnormality of the upper limb [HP:0002817] <20>(26|29) (30|18|16)
+ + + 3:   Aplasia/hypoplasia involving bones of the extremities [HP:0045060] <3>(7|8) (8|3|5)
+ + + 3:   Abnormality of limb bone morphology [HP:0002813] <13>(28|30) (30|18|20)
+ + 2:   Abnormal digit morphology [HP:0011297] <10>(16|19) (17|14|16)
+ + 2:   Aplasia/hypoplasia involving bones of the upper limbs [HP:0006496] <8>(3|8) (6|2|4)
+ + 2:   Abnormality of the hand [HP:0001155] <26>(20|25) (24|16|14)
+ 1:   Abnormality of finger [HP:0001167] <24>(11|14) (12|10|10)
+ 1:   Aplasia/hypoplasia involving bones of the hand [HP:0005927] <6>(3|6) (6|2|4)
0:   Aplasia/Hypoplasia of fingers [HP:0006265] <9>(2|3) (2|1|3)
- 1:   Aplasia of the fingers [HP:0009380] <10>(0|0) (0|0|0)
- 1:   Short finger [HP:0009381] <8>(2|3) (2|1|3)
- 1:   Aplasia/Hypoplasia of the 5th finger [HP:0006262] <3>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the thumb [HP:0009601] <3>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the 2nd finger [HP:0006264] <2>(0|1) (0|0|0)
- 1:   Aplasia/Hypoplasia of the 3rd finger [HP:0009318] <2>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the 4th finger [HP:0009272] <2>(0|0) (0|0|0)
- 1:   Proportionate shortening of all digits [HP:0006165](0|0) (0|0|0)
- 1:   Small finger [HP:0030033](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
ARID-like0.0001721Direct
Multidrug efflux transporter AcrB transmembrane domain0.001507Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
ARID domain0.0001033Direct
Transforming growth factor (TGF)-beta0.4299Inherited
Homeodomain0.6147Inherited


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-like0.00008434Direct
Multidrug efflux transporter AcrB transmembrane domain0.0008422Direct

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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
  • 0.00825Inherited

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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
  • 0.001905Inherited
    57196,57184,57184
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 57184 - Growth factor receptor domain
  • 0.005212Inherited


    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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