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Phenotypic Abnormality (PA): Aplasia/Hypoplasia of the patella

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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 skeletal morphology [HP:0011842] <18>(87|89) (90|49|32)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the skeletal system [HP:0000924] <7>(89|98) (94|51|33)
+ + + + 4:   Abnormality of limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + + + 4:   Aplasia/hypoplasia involving the skeleton [HP:0009115] <2>(13|11) (13|10|17)
+ + + + 4:   Abnormality of limb bone [HP:0040068] <1>(28|30) (30|18|20)
+ + + + 4:   Abnormal joint morphology [HP:0001367] <18>(18|22) (20|9|2)
+ + + + 4:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|41) (38|23|23)
+ + + 3:   Abnormality of lower limb joint [HP:0100491] <5>(10|12) (11|2|1)
+ + + 3:   Aplasia/hypoplasia of the extremities [HP:0009815] <6>(8|9) (9|3|5)
+ + + 3:   Abnormality of limb bone morphology [HP:0002813] <13>(28|30) (30|18|20)
+ + + 3:   Abnormality of the lower limb [HP:0002814] <17>(30|31) (33|14|13)
+ + 2:   Abnormality of the knee [HP:0002815] <15>(3|4) (4|1|1)
+ + 2:   Abnormal lower limb bone morphology [HP:0040069] <10>(10|8) (11|5|6)
+ + 2:   Aplasia/hypoplasia involving bones of the extremities [HP:0045060] <3>(7|8) (8|3|5)
+ 1:   Aplasia/hypoplasia involving bones of the lower limbs [HP:0006493] <10>(5|4) (5|3|4)
+ 1:   Abnormal patella morphology [HP:0003045] <10>(2|2) (2|0|0)
0:   Aplasia/Hypoplasia of the patella [HP:0006498] <2>(0|0) (1|0|0)
- 1:   Patellar aplasia [HP:0006443](0|0) (0|0|0)
- 1:   Patellar hypoplasia [HP:0003065](0|0) (0|0|0)


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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
ARID-like0.0008501Direct


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