Unified phenotype ontology (uPheno)
12991 terms(s) returned
Term Type: Class | Record: 1 to 50 of 12991 Records | Page: 1 of 260, First Previous Next Last | Show Records Per Page |
- P cell cleavage delayed
- P cell misalignment at ventral midline
- P granule
- P granule abnormal
- P granule blastomere decreased size, abnormal
- P granule degradation defective
- P granule localization defective
- P granule number abnormal
- P granule number reduced
- P granule phenotype
- P granule primordial germ cell decreased amount, abnormal
- P granule primordial germ cell physical object quality, abnormal
- P granule primordial germ cell size, abnormal
- P lineage cell
- P lineages variant
- P mitrale
- P pulmonale
- P wave inversion
- P-P-bond-hydrolysis-driven transmembrane transporter activity phenotype
- P-body
- P-stage
- P-type ion transporter activity
- P-type potassium transmembrane transporter activity
- P-type sodium transporter activity
- P-type sodium:potassium-exchanging transporter activity
- P-type sodium:potassium-exchanging transporter activity decreased occurrence, abnormal
- P-type transmembrane transporter activity
- P0
- P0 spindle absent early emb
- P0 spindle position abnormal
- P0 spindle rotation delayed early emb
- P0 spindle rotation failure early emb
- P1
- P1 aster defective early emb
- P2 EMS synchronous division early emb
- P4 lineage variant
- P7.pppp
- PAH (human)
- PHIPO_0000505
- PHso1L
- PLANP_00000000
- PML body
- PML body phenotype
- PNS synaptic transmission trait
- PP cell
- PP cell of intestine
- PP cell phenotype
- PR segment depression
- PR segment elevation
- PRL (human)