Phenotypic Abnormality (PA): Photophobia

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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)
+ + + 3:	Abnormality of the nervous system [HP:0000707] <4>	(142|168)	(156|103|45)
+ + 2:	Abnormality of nervous system physiology [HP:0012638] <26>	(101|119)	(112|81|39)
+ + 2:	Abnormal eye physiology [HP:0012373] <17>	(34|47)	(37|22|20)
+ 1:	Behavioral abnormality [HP:0000708] <38>	(17|24)	(19|15|5)
+ 1:	Abnormality of vision [HP:0000504] <15>	(4|16)	(9|8|8)
0:	Photophobia [HP:0000613]	(1|3)	(1|0|0)

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Superfamily

Superfamily domains annotated to this HP term (Not in SDHP)
Highlighted in gray are those with FDR_all>0.001

SCOP term	FDR (all)	Annotation (direct or inherited)
cAMP-binding domain-like	0.0002088	DIRECT

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Family

Family domains annotated to this HP term (SDHP level: Highly Informative)
Highlighted in gray are those with FDR_all>0.001

SCOP term	FDR (all)	Annotation (direct or inherited)
Pyrin domain, PYD	0.0003384	DIRECT
cAMP-binding domain	0.0006441	DIRECT
28-residue LRR	0.0006514	DIRECT

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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)
cAMP-binding domain-like	0.0001004	DIRECT