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Mammalian Phenotype (MP): abnormal enteric neuron 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)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + 2:   abnormal nervous system morphology [MP:0003632] <17>(76|104) (91|64|47)
+ + 2:   abnormal autonomic nervous system morphology [MP:0002751] <3>(4|5) (4|0|0)
+ 1:   abnormal enteric nervous system morphology [MP:0001044] <4>(0|1) (0|0|0)
+ 1:   abnormal neuron morphology [MP:0002882] <29>(36|59) (40|26|19)
0:   abnormal enteric neuron morphology [MP:0001046] <2>(0|1) (0|0|0)
- 1:   abnormal enteric cholinergic neuron morphology [MP:0001047] <1>(0|0) (0|0|0)
- 1:   absent enteric neurons [MP:0001048](0|0) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Transforming growth factor (TGF)-beta0.0005179Direct


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