Phenotypic Abnormality (PA): Aplasia/Hypoplasia involving the musculature of the extremities

---

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)
+ + + 3:	Abnormality of the musculature [HP:0003011] <3>	(64|83)	(70|33|9)
+ + + 3:	Phenotypic abnormality [HP:0000118] <25>
+ + 2:	Abnormality of limbs [HP:0040064] <8>	(58|66)	(63|33|25)
+ + 2:	Abnormality of muscle size [HP:0030236] <3>	(6|6)	(6|3|0)
+ + 2:	Abnormal skeletal muscle morphology [HP:0011805] <38>	(30|36)	(35|14|4)
+ 1:	Abnormality of the musculature of the limbs [HP:0009127] <10>	(12|11)	(16|5|3)
+ 1:	Aplasia/Hypoplasia involving the skeletal musculature [HP:0001460] <3>	(2|2)	(2|1|0)
0:	Aplasia/Hypoplasia involving the musculature of the extremities [HP:0009128] <2>	(0|0)	(0|0|0)
- 1:	Aplasia/Hypoplasia involving the musculature of the upper limbs [HP:0001467] <3>	(0|0)	(0|0|0)
- 1:	Aplasia/Hypoplasia of the musculature of the thigh [HP:0009786] <1>	(0|0)	(0|0|0)

---