All individuals with variants in gene MYO18B

5 entries on 1 page. Showing entries 1 - 5.
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     
00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 1 1 Yu Sun
00017599 - PubMed: Casey 2014 2-generation family, 1 affected, unaffected heterozygous carrier mother M yes Ireland Irish Traveller - - - - CILD see paper; normal situs, EM revealed that, typically, both inner and outer dynein arms are absent 1 1 Johan den Dunnen
00104015 Vogelaar-520A PubMed: Vogelaar 2017, Journal: Vogelaar 2017 54 patients from 53 families with genetically unexplained diffuse-type and intestinal-type gastric cancer - - - - - - - - cancer, gastric diffuse-type or intestinal-type gastric cancer 1 1 Marjolijn JL Ligtenberg
00293078 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 15 Mohammed Faruq
00307213 D17-0045 PubMed: Ravenscroft 2020, Journal: Ravenscroft 2020 - - - Australia - - - - - FADS antenatal onset; hypoplasia musculature; elbow flexion contracture; knee flexion contracture; hip contracture; pterygium; cystic hygroma; dextrotransposition great arteries; ventricular septal defect hypoplastic left heart; abnormal cerebral morphology 2 1 Gianina Ravenscroft
Legend   How to query  


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