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Phenotypic Abnormality (PA): Aplasia/Hypoplasia of the phalanges of the hand

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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:   Abnormality of skeletal morphology [HP:0011842] <18>(87|89) (90|49|32)
+ + + + + + 6:   Abnormality of the skeletal system [HP:0000924] <7>(89|98) (94|51|33)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of limb bone [HP:0040068] <1>(28|30) (30|18|20)
+ + + + + 5:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|41) (38|23|23)
+ + + + + 5:   Abnormality of limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + + + 4:   Abnormality of limb bone morphology [HP:0002813] <13>(28|30) (30|18|20)
+ + + + 4:   Abnormality of the upper limb [HP:0002817] <20>(26|29) (30|18|16)
+ + + 3:   Abnormality of the hand [HP:0001155] <26>(20|25) (24|16|14)
+ + + 3:   Abnormal digit morphology [HP:0011297] <10>(16|19) (17|14|16)
+ + 2:   Abnormality of finger [HP:0001167] <24>(11|14) (12|10|10)
+ 1:   Abnormal finger phalanx morphology [HP:0005918] <24>(7|8) (7|6|3)
0:   Aplasia/Hypoplasia of the phalanges of the hand [HP:0009767] <11>(3|3) (3|2|3)
- 1:   Short phalanx of finger [HP:0009803] <5>(2|2) (2|2|3)
- 1:   Aplasia/Hypoplasia of the phalanges of the thumb [HP:0009658] <4>(0|0) (0|0|0)
- 1:   Aplasia of the phalanges of the hand [HP:0009802] <3>(0|1) (0|0|0)
- 1:   Aplasia/Hypoplasia of the distal phalanges of the hand [HP:0009835] <3>(2|1) (2|0|0)
- 1:   Aplasia/Hypoplasia of the phalanges of the 2nd finger [HP:0009552] <3>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the phalanges of the 3rd finger [HP:0009447] <3>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the phalanges of the 4th finger [HP:0009408] <3>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the phalanges of the 5th finger [HP:0009376] <3>(1|1) (1|0|0)
- 1:   Aplasia/Hypoplasia of the middle phalanges of the hand [HP:0009843] <2>(1|1) (1|0|0)
- 1:   Aplasia/Hypoplasia of the proximal phalanges of the hand [HP:0009851] <2>(0|0) (0|0|0)
- 1:   Aphalangy of the hands [HP:0005886] <1>(0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
ARID-like0.00004571Direct
Multidrug efflux transporter AcrB transmembrane domain0.0005714Direct
Cystine-knot cytokines0.05273Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
ARID domain0.00002622Direct
Transforming growth factor (TGF)-beta0.04077Inherited
I set domains0.1832Inherited


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-like0.00002129Direct
Multidrug efflux transporter AcrB transmembrane domain0.0002991Direct
Cystine-knot cytokines0.03941Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57903,57903
  • 57903 - FYVE/PHD zinc finger
  • 57903 - FYVE/PHD zinc finger
  • 0.0007691Direct
    57196,57184
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.05258Inherited

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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
  • 0.0000707Direct
    57196,57196,57184
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.01686Inherited
    57196,57184,57184
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 57184 - Growth factor receptor domain
  • 0.03406Inherited


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