Phenotypic Abnormality (PA): Telangiectasia of the ear

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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:	Abnormality of the integument [HP:0001574] <4>	(48|69)	(59|37|15)
+ + + + + + 6:	Abnormality of the skin [HP:0000951] <4>	(34|55)	(45|36|12)
+ + + + + 5:	Abnormality of skin morphology [HP:0011121] <22>	(29|49)	(40|31|11)
+ + + + + 5:	Abnormality of the cardiovascular system [HP:0001626] <5>	(60|88)	(73|43|30)
+ + + + 4:	Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:	Abnormality of the vasculature [HP:0002597] <13>	(35|56)	(45|27|18)
+ + + + 4:	Generalized abnormality of skin [HP:0011354] <12>	(8|12)	(12|4|1)
+ + + 3:	Abnormality of the ear [HP:0000598] <2>	(17|32)	(21|13|11)
+ + + 3:	Vascular skin abnormality [HP:0011276] <10>	(6|10)	(9|2|1)
+ + 2:	Telangiectasia [HP:0001009] <6>	(1|2)	(1|0|0)
+ + 2:	Abnormal ear morphology [HP:0031703] <5>	(15|26)	(18|11|10)
+ 1:	Abnormality of the outer ear [HP:0000356] <14>	(6|7)	(7|3|1)
+ 1:	Telangiectasia of the skin [HP:0100585] <10>	(0|0)	(0|0|0)
0:	Telangiectasia of the ear [HP:0009893]	(0|0)	(0|0|0)

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