All individuals with variants in gene CCDC103

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00001636 - PubMed: Lines 2012 - F no - - - - - - MFDGA;MFDM IUGR; Malar hypoplasia; Micrognathia; Upslanting of obliquity of palpebrae; Microtia; Unilateral preauricular tags; Unilateral auditory canal atresia/stenosis; Conductive hearing loss; Midline cleft palate; Moderate to severe global developmental delay; Walking at 24-36m; Congenital heart defect(VSD; 46,XX; no seizures 1 1 Johan den Dunnen
00081098 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - CILD17 Ciliary dyskinesia, primary, 17 (OMIM:614679) 1 1 Daniel Trujillano
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.