Phenotypic Abnormality (PA): Lymphangioma

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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)
+ + + 3:	Neoplasm [HP:0002664] <2>	(20|21)	(23|8|3)
+ + + 3:	Abnormality of the cardiovascular system [HP:0001626] <5>	(60|88)	(73|43|30)
+ + + 3:	Phenotypic abnormality [HP:0000118] <25>
+ + 2:	Abnormality of the vasculature [HP:0002597] <13>	(35|56)	(45|27|18)
+ + 2:	Neoplasm by histology [HP:0011792] <7>	(5|7)	(6|3|0)
+ + 2:	Abnormality of the immune system [HP:0002715] <3>	(38|52)	(40|29|16)
+ 1:	Hamartoma [HP:0010566] <10>	(0|0)	(0|0|0)
+ 1:	Abnormality of the lymphatic system [HP:0100763] <7>	(9|19)	(15|8|5)
0:	Lymphangioma [HP:0100764] <2>	(0|0)	(0|0|0)
- 1:	Lymphangioma of the orbit [HP:0500091]	(0|0)	(0|0|0)
- 1:	Mediastinal cystic lymphangioma [HP:0030785]	(0|0)	(0|0|0)

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