Phenotypic Abnormality (PA): Heteronymous hemianopia

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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:	Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:	Abnormality of the eye [HP:0000478] <2>	(64|78)	(69|38|28)
+ + + + + 5:	Abnormal eye physiology [HP:0012373] <17>	(34|47)	(37|22|20)
+ + + + 4:	Abnormality of vision [HP:0000504] <15>	(4|16)	(9|8|8)
+ + + 3:	Visual impairment [HP:0000505] <4>	(0|8)	(3|6|7)
+ + 2:	Visual field defect [HP:0001123] <9>	(0|4)	(1|2|0)
+ 1:	Hemianopia [HP:0012377] <2>	(0|1)	(1|1|0)
0:	Heteronymous hemianopia [HP:0030517] <3>	(0|0)	(0|0|0)
- 1:	Binasal hemianopia [HP:0030520]	(0|0)	(0|0|0)
- 1:	Bitemporal hemianopia [HP:0030521]	(0|0)	(0|0|0)
- 1:	Congruous heteronymous hemianopia [HP:0030519]	(0|0)	(0|0|0)

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