Phenotypic Abnormality (PA): Optic atrophy

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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 morphology [HP:0012372] <12>	(39|48)	(41|29|22)
+ + + + 4:	Abnormal posterior eye segment morphology [HP:0004329] <3>	(16|11)	(17|6|8)
+ + + 3:	Abnormal fundus morphology [HP:0001098] <10>	(15|11)	(16|6|8)
+ + 2:	Abnormality of the optic nerve [HP:0000587] <14>	(4|5)	(4|1|0)
+ 1:	Abnormality of the optic disc [HP:0012795] <6>	(1|3)	(1|0|0)
0:	Optic atrophy [HP:0000648] <1>	(1|2)	(1|0|0)
- 1:	Optic atrophy from cranial nerve compression [HP:0007958]	(0|0)	(0|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)
Nucleotide-diphospho-sugar transferases	0.0009023	DIRECT

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Family

Family 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)
Ferredoxin domains from multidomain proteins	0	DIRECT
IF2B-like	0	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)
Nucleotide-diphospho-sugar transferases	0.0004752	DIRECT