Activity
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| Respiratory ciliopathies including non-CF bronchiectasis v4.28 | DNAH10 |
Achchuthan Shanmugasundram changed review comment from: The ClinGen Motile Ciliopathy expert panel has classified the association of autosomal recessive DNAH10 variants to ciliary dyskinesia (MONDO:0016575) as 'Limited'. More information can be found in https://search.clinicalgenome.org/CCID:008793. Sources: ClinGen; to: The ClinGen Motile Ciliopathy expert panel has classified the association of autosomal recessive DNAH10 variants to primary ciliary dyskinesia (MONDO:0016575) as 'Limited'. More information can be found in https://search.clinicalgenome.org/CCID:008793. Sources: ClinGen |
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| Respiratory ciliopathies including non-CF bronchiectasis v4.26 | DNAH10 |
Achchuthan Shanmugasundram changed review comment from: The ClinGen Motile Ciliopathy expert panel has classified the association of autosomal recessive DNAH10 variants to ciliary dyskinesia (MONDO:0016575) as 'Limited'. Please see https://search.clinicalgenome.org/CCID:008793 for more information. Sources: ClinGen; to: The ClinGen Motile Ciliopathy expert panel has classified the association of autosomal recessive DNAH10 variants to ciliary dyskinesia (MONDO:0016575) as 'Limited'. More information can be found in https://search.clinicalgenome.org/CCID:008793. Sources: ClinGen |
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| Respiratory ciliopathies including non-CF bronchiectasis v4.26 | DNAH10 |
Achchuthan Shanmugasundram gene: DNAH10 was added gene: DNAH10 was added to Respiratory ciliopathies including non-CF bronchiectasis. Sources: ClinGen Mode of inheritance for gene: DNAH10 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: DNAH10 were set to Spermatogenic failure 56, OMIM:619515; primary ciliary dyskinesia, MONDO:0016575 Review for gene: DNAH10 was set to RED Added comment: The ClinGen Motile Ciliopathy expert panel has classified the association of autosomal recessive DNAH10 variants to ciliary dyskinesia (MONDO:0016575) as 'Limited'. Please see https://search.clinicalgenome.org/CCID:008793 for more information. Sources: ClinGen |
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