Phenotypic Abnormality (PA): Abnormality of the pulmonary artery

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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)
+ + + + 4:	Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:	Abnormality of the respiratory system [HP:0002086] <3>	(30|35)	(38|24|21)
+ + + 3:	Abnormal respiratory system morphology [HP:0012252] <5>	(20|25)	(26|18|17)
+ + + 3:	Abnormality of the cardiovascular system [HP:0001626] <5>	(60|88)	(73|43|30)
+ + 2:	Abnormal lung morphology [HP:0002088] <28>	(11|18)	(18|11|7)
+ + 2:	Abnormality of the vasculature [HP:0002597] <13>	(35|56)	(45|27|18)
+ 1:	Abnormality of the pulmonary vasculature [HP:0004930] <6>	(1|0)	(3|2|3)
0:	Abnormality of the pulmonary artery [HP:0004414] <2>	(0|0)	(0|1|2)
- 1:	Abnormal pulmonary artery morphology [HP:0030966] <10>	(0|0)	(0|0|1)
- 1:	Abnormal pulmonary artery physiology [HP:0030967] <1>	(0|0)	(0|0|0)

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Supra-domain (including individual superfamily)

Supra-domains annotated to this HP term (SPHO level: Highly Informative)
Highlighted in gray are those with FDR>0.001

Supra-domain (Duplex) in N- to C-terminal order	FDR (all)	Annotation (direct or inherited)
57184,57184 57184 - Growth factor receptor domain 57184 - Growth factor receptor domain	0.000002316	DIRECT

Supra-domains annotated to this HP term (SPHO level: Highly Informative)
Highlighted in gray are those with FDR>0.001

Supra-domain (Triple) in N- to C-terminal order	FDR (all)	Annotation (direct or inherited)
57196,57184,57184 57196 - EGF/Laminin 57184 - Growth factor receptor domain 57184 - Growth factor receptor domain	0.000002383	DIRECT
57184,57184,57196 57184 - Growth factor receptor domain 57184 - Growth factor receptor domain 57196 - EGF/Laminin	0.000004821	DIRECT

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