OBO ID: DOID:0112176 |
Term Name: | spermatogenic failure 48 | Search Ontology: | |
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Synonyms: |
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Definition: | A spermatogenic failure that is characterized by impaired spermatogenesis, primarily occurring at meiosis that has_material_basis_in homozygous or compound heterozygous mutation in M1AP on chromosome 2p13.1. (2) | ||
References: | |||
Ontology: | Human Disease ( DOID:0112176 ) |
OTHER spermatogenic failure 48 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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