Phenotypic Abnormality (PA): Partial absence of foot

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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] <17>	(86|89)	(90|52|33)
+ + + + + + 6:	Abnormality of the skeletal system [HP:0000924] <7>	(88|98)	(93|55|34)
+ + + + + 5:	Abnormality of limb bone [HP:0040068] <1>	(29|32)	(33|18|20)
+ + + + + 5:	Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:	Aplasia/hypoplasia involving the skeleton [HP:0009115] <2>	(13|12)	(15|10|17)
+ + + + + 5:	Abnormal appendicular skeleton morphology [HP:0011844] <4>	(35|43)	(39|23|23)
+ + + + 4:	Abnormality of limb bone morphology [HP:0002813] <13>	(29|32)	(32|18|20)
+ + + + 4:	Abnormality of limbs [HP:0040064] <8>	(58|66)	(63|33|25)
+ + + + 4:	Aplasia/hypoplasia of the extremities [HP:0009815] <6>	(8|10)	(10|3|5)
+ + + 3:	Abnormality of the lower limb [HP:0002814] <17>	(31|34)	(35|15|13)
+ + + 3:	Abnormal lower limb bone morphology [HP:0040069] <10>	(11|9)	(12|5|6)
+ + + 3:	Aplasia/hypoplasia involving bones of the extremities [HP:0045060] <3>	(7|9)	(9|3|5)
+ + 2:	Aplasia/hypoplasia involving bones of the lower limbs [HP:0006493] <10>	(5|5)	(6|3|4)
+ + 2:	Abnormality of the foot [HP:0001760] <30>	(20|24)	(21|13|10)
+ 1:	Aplasia/Hypoplasia involving bones of the feet [HP:0006494] <8>	(4|4)	(5|2|3)
0:	Partial absence of foot [HP:0030032]	(0|0)	(0|0|0)

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