Mammalian Phenotype (MP): abnormal type III spiral ligament fibrocytes

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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:	mammalian phenotype [MP:0000001] <29>
+ + + + + + + 7:	hearing/vestibular/ear phenotype [MP:0005377] <2>	(20|24)	(23|14|5)
+ + + + + + 6:	abnormal ear morphology [MP:0002102] <4>	(16|21)	(18|14|5)
+ + + + + 5:	skeleton phenotype [MP:0005390] <2>	(46|63)	(50|41|26)
+ + + + + 5:	abnormal inner ear morphology [MP:0000026] <15>	(13|15)	(13|11|5)
+ + + + + 5:	abnormal membranous labyrinth morphology [MP:0000035] <2>	(11|14)	(12|9|5)
+ + + + 4:	abnormal cochlea morphology [MP:0000031] <15>	(12|14)	(13|8|5)
+ + + + 4:	abnormal skeleton morphology [MP:0005508] <15>	(41|59)	(47|38|25)
+ + + + 4:	abnormal cochlear labyrinth morphology [MP:0004426] <1>	(10|12)	(11|8|5)
+ + + 3:	abnormal ligament morphology [MP:0005504] <5>	(2|2)	(2|1|0)
+ + + 3:	abnormal scala media morphology [MP:0003169] <9>	(10|12)	(11|8|5)
+ + 2:	abnormal spiral ligament morphology [MP:0004288] <3>	(2|2)	(2|1|0)
+ 1:	abnormal spiral ligament fibrocyte morphology [MP:0004292] <4>	(2|2)	(2|1|0)
0:	abnormal type III spiral ligament fibrocytes [MP:0004295] <1>	(0|0)	(0|0|0)
- 1:	type III spiral ligament fibrocyte degeneration [MP:0004489]	(0|0)	(0|0|0)

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