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Phenotypic Abnormality (PA): Short middle phalanx of finger

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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)
+ + + + + + + 7:   Aplasia/hypoplasia involving the skeleton [HP:0009115] <2>(13|11) (13|10|17)
+ + + + + + 6:   Aplasia/hypoplasia of the extremities [HP:0009815] <6>(8|9) (9|3|5)
+ + + + + + 6:   Abnormality of skeletal morphology [HP:0011842] <18>(87|89) (90|49|32)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Abnormality of the skeletal system [HP:0000924] <7>(89|98) (94|51|33)
+ + + + + 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:   Aplasia/hypoplasia involving bones of the extremities [HP:0045060] <3>(7|8) (8|3|5)
+ + + + + 5:   Abnormality of limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + + + 4:   Abnormality of the upper limb [HP:0002817] <20>(26|29) (30|18|16)
+ + + + 4:   Aplasia/hypoplasia involving bones of the upper limbs [HP:0006496] <8>(3|8) (6|2|4)
+ + + + 4:   Abnormality of limb bone morphology [HP:0002813] <13>(28|30) (30|18|20)
+ + + 3:   Aplasia/hypoplasia involving bones of the hand [HP:0005927] <6>(3|6) (6|2|4)
+ + + 3:   Abnormality of the hand [HP:0001155] <26>(20|25) (24|16|14)
+ + + 3:   Abnormal finger phalanx morphology [HP:0005918] <24>(7|8) (7|6|3)
+ + + 3:   Abnormality of finger [HP:0001167] <24>(11|14) (12|10|10)
+ + + 3:   Abnormal digit morphology [HP:0011297] <10>(16|19) (17|14|16)
+ + 2:   Aplasia/Hypoplasia of fingers [HP:0006265] <9>(2|3) (2|1|3)
+ + 2:   Short digit [HP:0011927] <3>(4|5) (4|4|4)
+ + 2:   Abnormal middle phalanx morphology of the hand [HP:0009833] <14>(1|1) (1|0|0)
+ + 2:   Aplasia/Hypoplasia of the phalanges of the hand [HP:0009767] <11>(3|3) (3|2|3)
+ + 2:   Abnormal hand morphology [HP:0005922] <11>(2|4) (2|2|4)
+ 1:   Short finger [HP:0009381] <8>(2|3) (2|1|3)
+ 1:   Short phalanx of finger [HP:0009803] <5>(2|2) (2|2|3)
+ 1:   Aplasia/Hypoplasia of the middle phalanges of the hand [HP:0009843] <2>(1|1) (1|0|0)
0:   Short middle phalanx of finger [HP:0005819] <6>(0|1) (0|0|0)
- 1:   Short middle phalanx of the 2nd finger [HP:0009577](0|0) (0|0|0)
- 1:   Short middle phalanx of the 3rd finger [HP:0009439](0|0) (0|0|0)
- 1:   Short middle phalanx of the 4th finger [HP:0009295](0|0) (0|0|0)
- 1:   Short middle phalanx of the 5th finger [HP:0004220](0|0) (0|0|0)
- 1:   Short proximal phalanx of thumb [HP:0009638](0|0) (0|0|0)
- 1:   Shortening of all middle phalanges of the fingers [HP:0006110](0|0) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Transforming growth factor (TGF)-beta0.0003234Direct


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