Simple categories matching chromosomal:

• anomaly,
• activity,
• change,
• mechanism,
• abnormality,
• level,
• investigation,
• event,
• alteration,
• aberration,
• rearrangement,
• protein,
• landmark,
• metabolism,
• mutation,
• disorder,
• integrity,
• feature,
• region,
• process,
• structure,
• fragment,

Members with property chromosomal:

• replication_bubble,
• aneuploidy,
• monosomy,
• dna_repair,
• inversion,
• aberration,
• transcription,
• loss,
• meiosis_formation,
• deletion,
• trisomy,
• chromosomal_losses,
• amplification,
• chromosome_alignment,
• histone,
• mutation,
• chromosomal_aneuploidy,
• recombination,
• factor-viii_inversion,
• gene_regulation,
• aberration_detection,
• nucleolus-organizer_region,
• transposable_elements,
• centromere,
• x_monosomy,
• breakage,
• reverse_transcription,
• irregular_shape,
• telomere,
• gene_activation,
• substitution,
• origin,
• telomere_attrition,
• kinetochore,
• mitotic_recombination,
• losses,
• dna_gain,
• chromosomal_aberration,
• small_deletion,
• chromosome_condensation,
• duplication_trisomy,
• frame_shift,
• nucleolar-organizer_region,
• minute_deletion,
• accessory_chromosome,
• segmental_duplication,
• gain,
• small_insertion,
• anencephaly,
• kinetochore_formation,
• large_deletion,
• crossover,
• replication_origin,
• irradiation,
• replication,
• sequence_inversion,
• duplication,
• ladder,
• gene_conversion,
• turner,
• dna_amplification,
• checkpoint_control,
• break,
• gene_amplification,
• insertion,
• dominant_disorder,
• chromosome_break,
• chromosomal_loss,
• insertion_sequence,
• radiation,
• segregation,
• horizontal_transfer,
• scaffold_protein,
• fusion,
• transposition,
• homozygous_deletion,
• deletion_monosomy,
• gene_transcription,
• genetic_disorder,
• mongolism,
• repair,
• abnormal_segregation,
• meiosis,
• regulation,
• presence,
• oxidative_stress,
• dna_replication,
• unequal_crossover,
• segregation_distortion,
• rearrangement,
• addition,
• gap,
• numerical_aberration,
• achondroplasia_dwarfism,