old cv term	FYPO ID
phenotype, abnormal actin cortical patch localization	FYPO:0000190
phenotype, abnormal telomere maintenance	FYPO:0000122
phenotype, accumulation of carbonylated proteins	FYPO:0000219
phenotype, accumulation of non-coding outer repeat transcripts	FYPO:0000220
phenotype, adhesion defects, cell-substrate adhesion, abolished	FYPO:0000010
phenotype, aerobic growth defects	FYPO:0001355
phenotype, cell cycle, G2 delay	FYPO:0000012
phenotype, cell morphology, branched	FYPO:0001512
phenotype, cell morphology, curved	FYPO:0000016
phenotype, cell morphology, elongated and multiseptate	FYPO:0000223
phenotype, cell morphology, elongated cells	FYPO:0001122
phenotype, cell morphology, elongated dumbbell	FYPO:0000779
phenotype, cell morphology, lemon shaped	FYPO:0000224
phenotype, cell morphology, misshapen cells	FYPO:0001118
phenotype, cell morphology, pear shaped	FYPO:0001120
phenotype, cell morphology, round cells	FYPO:0000021
phenotype, cell morphology, small cells	FYPO:0000645
phenotype, cell morphology, stubby cells	FYPO:0000024
phenotype, cell morphology, swollen cells	FYPO:0000646
phenotype, cell morphology, T shaped	FYPO:0000013
phenotype, cell polarity defects	FYPO:0000026
phenotype, chromosome condensation defects	FYPO:0000159
phenotype, chromosome segregation defects	FYPO:0000029
phenotype, chromosome segregation defects, chromosome fragmentation	FYPO:0000283
phenotype, chromosome segregation defects, chromosome loss	FYPO:0000227
phenotype, chromosome segregation defects, lagging chromosomes	FYPO:0000228
phenotype, chromosome segregation defects, mitotic	FYPO:0000141
phenotype, colony morphology, flocculation	FYPO:0000155
phenotype, conjugation defects	FYPO:0000031
phenotype, cut	FYPO:0003165
phenotype, cytokinesis defects	FYPO:0000032
phenotype, cytokinesis defects, contractile ring actin, absent	FYPO:0001008
phenotype, cytokinesis defects, contractile ring myosin distribution, defective	FYPO:0000231
phenotype, cytokinesis defects, splitting of the actinomyosin ring	FYPO:0000232
phenotype, defective in recovery of translation after hyperosmotic shock	FYPO:0000235
phenotype, defective in recovery of translation after oxidative stress	FYPO:0000236
phenotype, defective in recovery of translation during nitrogen starvation	FYPO:0000237
phenotype, DNA damage checkpoint defects	FYPO:0000006
phenotype, DNA damage checkpoint defects, S-phase	FYPO:0000007
phenotype, DNA fragmentation	FYPO:0000160
phenotype, DNA recombination defect, at mitotic DNA replication fork barriers, elevated	FYPO:0000167
phenotype, DNA recombination defects, crossover, abolished	FYPO:0000181
phenotype, DNA recombination defects, gene conversion, reduced	FYPO:0000185
phenotype, DNA recombination defects, long tract gene conversion, increased	FYPO:0000199
phenotype, DNA recombination defects, meiotic	FYPO:0000008
phenotype, DNA replication defects, endoreduplication	FYPO:0000216
phenotype, endocytosis defects	FYPO:0000034
phenotype, expression of MBF target genes increased	FYPO:0000239
phenotype, filament morphology aberrant	FYPO:0000240
phenotype, glucan synthesis defective	FYPO:0000043
phenotype, glucose repression defects	FYPO:0000044
phenotype, growth defect, normal growth with ammonia nitrogen source	FYPO:0000242
phenotype, growth defect, normal growth with proline nitrogen source	FYPO:0000243
phenotype, growth defect, slow growth	FYPO:0001234
phenotype, growth defect, slow growth at high temperatures	FYPO:0000247
phenotype, growth defect, slow growth in minimal media	FYPO:0000249
phenotype, growth defect, slow growth with ammonia nitrogen source	FYPO:0000249
phenotype, growth defect, slow growth with proline nitrogen source	FYPO:0000250
phenotype, growth defects, growth inhibition in galactose-based medium	FYPO:0000251
phenotype, growth normal	FYPO:0001357
phenotype, increased HMG-CoA reductase activity	FYPO:0000253
phenotype, invasive growth, abolished	FYPO:0000551
phenotype, inviable	FYPO:0002061
phenotype, kinetochore defects	FYPO:0000050
phenotype, localization defective, cytoplasmic	FYPO:0000783
phenotype, localization defects, sterol distribution defects	FYPO:0000135
phenotype, meiosis defects	FYPO:0000051
phenotype, microtubule organization defects	FYPO:0001350
phenotype, mitochondria fused	FYPO:0000056
phenotype, mitochondrial nucleoid enlarged	FYPO:0000057
phenotype, mitochondrial nucleoid reduced number	FYPO:0000058
phenotype, mononucleate	FYPO:0000060
phenotype, MRN complex formation, reduced	FYPO:0000218
phenotype, mutator	FYPO:0000256
phenotype, nuclear morphology defects	FYPO:0000062
phenotype, periodic cell-cycle expression, abolished	FYPO:0000260
phenotype, resistance to 5-azacytidine (nucleoside analogue)	FYPO:0000065
phenotype, resistance to AZC	FYPO:0000066
phenotype, resistance to caffeine	FYPO:0000072
phenotype, resistance to rapamycin	FYPO:0000077
phenotype, respiration defective	FYPO:0000078
phenotype, sensitive to 6-azauracil	FYPO:0000084
phenotype, sensitive to arsenic	FYPO:0000093
phenotype, sensitive to benomyl	FYPO:0000094
phenotype, sensitive to cadmium	FYPO:0000096
phenotype, sensitive to caffeine	FYPO:0000097
phenotype, sensitive to calcium	FYPO:0000098
phenotype, sensitive to cisplatin	FYPO:0000102
phenotype, sensitive to cold	FYPO:0000080
phenotype, sensitive to CPT	FYPO:0000085
phenotype, sensitive to glucan synthate inhibitor	FYPO:0000079
phenotype, sensitive to glucan synthate inhibitor	FYPO:0000083
phenotype, sensitive to H202	FYPO:0000087
phenotype, sensitive to high temperature	FYPO:0000082
phenotype, sensitive to HU	FYPO:0000088
phenotype, sensitive to latrunculin A	FYPO:0000107
phenotype, sensitive to MMS	FYPO:0000089
phenotype, sensitive to N-ethylmaleimide	FYPO:0000090
phenotype, sensitive to osmotic stress	FYPO:0000270
phenotype, sensitive to pravastatin	FYPO:0000110
phenotype, sensitive to salt stress	FYPO:0000271
phenotype, sensitive to tacrolimus	FYPO:0000086
phenotype, sensitive to TBZ	FYPO:0000091
phenotype, sensitive to UV	FYPO:0000268
phenotype, sensitive to valproic acid	FYPO:0000115
phenotype, sensitive to zinc	FYPO:0000116
phenotype, septation defects	FYPO:0000117
phenotype, septum initiation defective	FYPO:0000272
phenotype, short mitotic spindles	FYPO:0000732
phenotype, spindle assembly abnormal	FYPO:0000177
phenotype, spindle checkpoint activated	FYPO:0000274
phenotype, spindle elongation defects	FYPO:0000131
phenotype, sporulation defects	FYPO:0000121
phenotype, sterile	FYPO:0000280
phenotype, telomere maintenance defects	FYPO:0000122
phenotype, vacoule organization defects, large vacuoles	FYPO:0000123
phenotype, viable	FYPO:0002060
phenotype, mitotic spindle defects	FYPO:0000338
phenotype, mitotic spindle defects, monopolar spindle	FYPO:0000276
phenotype, DNA damage checkpoint override in response to caffeine abolished	FYPO:0000701
phenotype, increased protein processing	FYPO:0000254