ClinGen Knowledge Base | Clinical Genome Resource

CCDC103

Name: CCDC103
HGNC ID: HGNC:32700
Cytogenetic Location: 17q21.31
Haploinsufficiency: Associated with Autosomal Recessive Phenotype

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CCDC103 - primary ciliary dyskinesia 17 | MONDO:0013854

Curated by	Classification	Date	Report
Gene Dosage Sensitivity	Gene Associated with Autosomal Recessive Phenotype	05/31/2017	View report

CCDC103

Curated by	Classification	Date	Report
Gene Dosage Sensitivity	Gene Associated with Autosomal Recessive Phenotype	05/31/2017	View report

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