Mammalian Phenotype (MP): abnormal photoreceptor connecting cilium morphology

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Root: MP Hierarchy (mammalian/mouse phenotype from MGI_4.41)

Shortest distance to current term (+ for parents, - for children)	MP term [MP ID] <#Children>	(#SF|#FA)	#Supra-domain (Single|Duplex|Triple)
+ + + + + + + + + 9:	vision/eye phenotype [MP:0005391] <2>	(43|53)	(50|27|17)
+ + + + + + + + 8:	abnormal eye morphology [MP:0002092] <23>	(39|49)	(46|25|15)
+ + + + + + + 7:	abnormal posterior eye segment morphology [MP:0005195] <4>	(21|24)	(23|14|8)
+ + + + + + 6:	abnormal ocular fundus morphology [MP:0002864] <2>	(19|23)	(21|14|8)
+ + + + + + 6:	mammalian phenotype [MP:0000001] <29>
+ + + + + 5:	cellular phenotype [MP:0005384] <6>	(95|116)	(103|56|31)
+ + + + + 5:	abnormal retina morphology [MP:0001325] <23>	(19|23)	(21|14|8)
+ + + + + 5:	nervous system phenotype [MP:0003631] <2>	(98|128)	(113|79|50)
+ + + + 4:	abnormal somatic nervous system morphology [MP:0002752] <7>	(34|47)	(37|25|14)
+ + + + 4:	abnormal retinal layer morphology [MP:0003727] <3>	(11|16)	(12|8|6)
+ + + + 4:	abnormal nervous system morphology [MP:0003632] <17>	(76|104)	(91|64|47)
+ + + + 4:	abnormal cell morphology [MP:0000358] <12>	(19|19)	(22|9|2)
+ + + 3:	abnormal somatic sensory system morphology [MP:0000959] <4>	(26|38)	(29|19|12)
+ + + 3:	abnormal retinal neuronal layer morphology [MP:0006069] <7>	(11|15)	(11|8|5)
+ + + 3:	abnormal cilium morphology [MP:0013202] <2>	(3|2)	(3|3|1)
+ + + 3:	abnormal neuron morphology [MP:0002882] <29>	(36|59)	(40|26|19)
+ + 2:	abnormal sensory neuron morphology [MP:0000965] <16>	(16|28)	(19|14|9)
+ + 2:	abnormal retinal photoreceptor layer morphology [MP:0003728] <1>	(4|7)	(5|3|2)
+ + 2:	abnormal primary cilium morphology [MP:0013203] <2>	(3|2)	(3|3|1)
+ 1:	abnormal retinal photoreceptor morphology [MP:0001004] <8>	(4|7)	(5|3|2)
+ 1:	abnormal nonmotile primary cilium morphology [MP:0013205] <7>	(2|2)	(2|2|1)
0:	abnormal photoreceptor connecting cilium morphology [MP:0014059]	(0|0)	(0|0|0)

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