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

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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) (15|10|17)
+ + + + + + 6:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + + + + 6:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Aplasia/hypoplasia of the extremities [HP:0009815] <6>(8|9) (10|3|5)
+ + + + + 5:   Aplasia/hypoplasia involving bones of the extremities [HP:0045060] <3>(7|8) (9|3|5)
+ + + + + 5:   Abnormality of limb bone [HP:0040068] <1>(29|31) (33|18|20)
+ + + + + 5:   Abnormal lower limb bone morphology [HP:0040069] <10>(11|9) (12|5|6)
+ + + + + 5:   Abnormality of limbs [HP:0040064] <8>(58|65) (63|33|25)
+ + + + + 5:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|42) (39|23|23)
+ + + + 4:   Aplasia/hypoplasia involving bones of the lower limbs [HP:0006493] <10>(5|5) (6|3|4)
+ + + + 4:   Abnormality of the lower limb [HP:0002814] <17>(31|34) (35|15|13)
+ + + + 4:   Abnormality of limb bone morphology [HP:0002813] <13>(29|31) (32|18|20)
+ + + 3:   Abnormality of the foot [HP:0001760] <30>(20|24) (21|13|10)
+ + + 3:   Aplasia/Hypoplasia involving bones of the feet [HP:0006494] <8>(4|4) (5|2|3)
+ + + 3:   Abnormal digit morphology [HP:0011297] <10>(16|20) (18|14|16)
+ + 2:   Aplasia/Hypoplasia of toe [HP:0001991] <3>(3|3) (4|2|2)
+ + 2:   Abnormality of toe [HP:0001780] <27>(6|7) (8|4|2)
+ 1:   Absent toe [HP:0010760] <9>(2|2) (3|1|1)
+ 1:   Abnormality of the hallux [HP:0001844] <10>(0|0) (1|0|0)
0:   Aplasia/Hypoplasia of the hallux [HP:0008362] <3>(0|0) (1|0|0)
- 1:   Aplasia/Hypoplasia of the phalanges of the hallux [HP:0010058] <4>(0|0) (0|0|0)
- 1:   Short hallux [HP:0010109] <1>(0|0) (1|0|0)
- 1:   Absent hallux [HP:0012386](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)
Cystine-knot cytokines0.000696Direct


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