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Phenotype ontology term - FYPO:0003603 - abnormal meiosis I

Term summary

ID
FYPO:0003603
Name
abnormal meiosis I
Ontology or CV name
Phenotype
Definition
A cellular process phenotype in which the first meiotic nuclear division is abnormal.

Parents

Annotation

Multi-locus phenotype

FYPO:0007756 - abnormal homologous chromosome segregation with collapsed spindle

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FYPO:0007080 - abnormal initial meiotic spindle pole body separation in meiosis I

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FYPO:0006770 - abnormal kinetochore disassembly during meiotic prophase I

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FYPO:0007081 - abolished initial meiotic spindle pole body separation in meiosis I

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FYPO:0003378 - abolished meiosis I

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FYPO:0007083 - meiotic spindle collapse

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FYPO:0007103 - spindle collapse during meiosis I

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FYPO:0007744 - spindle collapse during meiotic prophase I

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Single locus phenotype

FYPO:0007756 - abnormal homologous chromosome segregation with collapsed spindle

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FYPO:0007080 - abnormal initial meiotic spindle pole body separation in meiosis I

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FYPO:0006770 - abnormal kinetochore disassembly during meiotic prophase I

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FYPO:0007081 - abolished initial meiotic spindle pole body separation in meiosis I

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FYPO:0003378 - abolished meiosis I

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FYPO:0005599 - increased duration of meiosis I

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FYPO:0007103 - spindle collapse during meiosis I

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FYPO:0007751 - spindle collapse during meiotic prometaphase I

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FYPO:0007752 - spindle regression during meiosis I

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