An emerging, recognizable facial phenotype in association with mutations in GLI-similar 3 (GLIS3)

Medicine and Dentistry

• Family 100%
• Diabetes 66%
• Congenital Hypothyroidism 66%
• Kidney 66%
• Phenotype 33%
• Diabetes Mellitus 33%
• Liver Disease 33%
• Nephropathy 33%
• Cholestasis 33%
• Glaucoma 33%
• Transcription Factor 33%
• Congenital Glaucoma 33%
• Kidney Function 33%
• Age 33%
• Hypothyroidism 33%
• Cyst 33%
• Liver Fibrosis 33%
• Polycystic Kidney Disease 33%
• Low Set Ear 33%
• Autoimmune Diabetes 33%
• Patient 33%
• Differentiation 33%
• Gene 33%
• Association 33%
• Photograph 33%
• Liver 33%
• Sibling 33%
• Syndrome 33%
• Intrauterine Growth Restriction 33%