Phenotypic Abnormality (PA): Abnormality of binocular vision

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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>
+ + + 3:	Abnormality of the eye [HP:0000478] <2>	(64|78)	(69|38|28)
+ + 2:	Abnormal eye physiology [HP:0012373] <17>	(34|47)	(37|22|20)
+ 1:	Abnormality of vision [HP:0000504] <15>	(4|16)	(9|8|8)
0:	Abnormality of binocular vision [HP:0011514] <2>	(0|0)	(2|1|0)
- 1:	Abnormal stereopsis [HP:0011515]	(0|0)	(0|0|0)
- 1:	Diplopia [HP:0000651]	(0|0)	(0|0|0)

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Supra-domain (including individual superfamily)

Supra-domains annotated to this HP term (Not in SPHO)
Highlighted in gray are those with FDR>0.001

Supra-domain (Single)	FDR (all)	Annotation (direct or inherited)
Nicotinic receptor ligand binding domain-like	0.0008325	DIRECT
Neurotransmitter-gated ion-channel transmembrane pore	0.0008325	DIRECT

Supra-domains annotated to this HP term (Not in SPHO)
Highlighted in gray are those with FDR>0.001

Supra-domain (Duplex) in N- to C-terminal order	FDR (all)	Annotation (direct or inherited)
63712,90112 63712 - Nicotinic receptor ligand binding domain-like 90112 - Neurotransmitter-gated ion-channel transmembrane pore	0.0008325	DIRECT