Mammalian Phenotype (MP): decreased thyrotroph cell number

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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>
+ + + + + + + + 8:	nervous system phenotype [MP:0003631] <2>	(98|128)	(113|79|50)
+ + + + + + + 7:	endocrine/exocrine gland phenotype [MP:0005379] <2>	(51|81)	(55|36|12)
+ + + + + + + 7:	abnormal nervous system morphology [MP:0003632] <17>	(76|104)	(91|64|47)
+ + + + + + 6:	abnormal gland morphology [MP:0002163] <8>	(44|71)	(50|31|11)
+ + + + + + 6:	abnormal brain morphology [MP:0002152] <24>	(25|42)	(35|24|14)
+ + + + + 5:	abnormal endocrine gland morphology [MP:0013560] <7>	(16|29)	(21|19|4)
+ + + + + 5:	abnormal forebrain morphology [MP:0000783] <8>	(18|26)	(24|15|8)
+ + + + 4:	abnormal neuroendocrine gland morphology [MP:0000631] <3>	(3|3)	(4|1|0)
+ + + + 4:	abnormal diencephalon morphology [MP:0000830] <11>	(4|5)	(6|1|0)
+ + + 3:	abnormal pituitary gland morphology [MP:0000633] <8>	(3|3)	(4|1|0)
+ + 2:	abnormal adenohypophysis morphology [MP:0004163] <12>	(2|2)	(3|1|0)
+ 1:	abnormal thyrotroph morphology [MP:0008326] <4>	(0|2)	(1|0|0)
0:	decreased thyrotroph cell number [MP:0008338] <1>	(0|1)	(0|0|0)
- 1:	absent thyrotrophs [MP:0008339]	(0|0)	(0|0|0)

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Family

Family domains annotated to this MP term (Not in SDMP)
Highlighted in gray are those with FDR_all>0.001

SCOP term	FDR (all)	Annotation (direct or inherited)
Homeodomain	0.000002345	DIRECT

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