Phenotypic Abnormality (PA): Lymphangiectasis

---

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)
+ + + + 4:	Abnormality of the cardiovascular system [HP:0001626] <5>	(60|88)	(73|43|30)
+ + + + 4:	Phenotypic abnormality [HP:0000118] <25>
+ + + 3:	Abnormality of cardiovascular system morphology [HP:0030680] <3>	(29|42)	(31|19|20)
+ + + 3:	Abnormality of the immune system [HP:0002715] <3>	(38|52)	(40|29|16)
+ + + 3:	Abnormality of the vasculature [HP:0002597] <13>	(35|56)	(45|27|18)
+ + 2:	Abnormality of the lymphatic system [HP:0100763] <7>	(9|19)	(15|8|5)
+ + 2:	Abnormal vascular morphology [HP:0025015] <12>	(15|18)	(16|11|10)
+ 1:	Abnormal lymphatic vessel morphology [HP:0100766] <5>	(0|0)	(0|0|0)
0:	Lymphangiectasis [HP:0031842] <6>	(0|0)	(0|0|0)
- 1:	Intestinal lymphangiectasia [HP:0002593]	(0|0)	(0|0|0)
- 1:	Pancreatic lymphangiectasis [HP:0006273]	(0|0)	(0|0|0)
- 1:	Pericardial lymphangiectasia [HP:0005183]	(0|0)	(0|0|0)
- 1:	Pleural lymphangiectasia [HP:0006531]	(0|0)	(0|0|0)
- 1:	Pulmonary lymphangiectasia [HP:0006521]	(0|0)	(0|0|0)
- 1:	Thyroid lymphangiectasia [HP:0008229]	(0|0)	(0|0|0)

---