Medicine and Dentistry
Chromosome 6
81%
Social Media
60%
Developmental Delay
31%
Clinician
24%
Identified Patient
18%
Chromosome Aberration
18%
Congenital Heart Defect
18%
Corpus Callosum
15%
Hypotonia
15%
Brain Abnormalities
13%
Congenital Disorder
13%
Foot Malformation
12%
Epileptic Seizure
12%
Autosome
9%
Gastrointestinal Distress
9%
Brain Malformation
9%
Advanced Life Support
9%
Hearing Impairment
9%
Haploinsufficiency
9%
Dysmorphic Feature
9%
Eye Movement
9%
Sleep Disorder
9%
Rare Disease
7%
Disease
7%
Chromosome Disorder
7%
Respiratory Tract Infection
6%
Ventriculomegaly
6%
Hypertelorism
6%
Cortical Dysplasia
6%
Hydrocephalus
6%
Outer Ear
6%
Muscle Hypertonia
6%
Spinal Dysraphism
6%
Hyperactivity
6%
Joint Laxity
6%
Microcephaly
6%
Ataxia
6%
Torticollis
6%
Vertebra
6%
Scoliosis
6%
Recurrent Infection
6%
Sleep
6%
Female Genitalia
6%
Bronchomalacia
6%
KCNQ5
6%
Eye Movement Disorder
6%
Feeding Difficulty
6%
Pervasive Developmental Disorder
6%
Gastroesophageal Reflux
6%
Hernia
6%
Biochemistry, Genetics and Molecular Biology
Chromosome 6
100%
Haploinsufficiency
40%
Microarrays
28%
Body Height
18%
Ephrin Receptor
18%
KCNQ5
18%
MAP3K7
18%
Eye Movement
15%
Autosome
9%
Chromosomal Disorder
7%
Exome Sequencing
6%
Dysplasia
6%
Sleep
6%
Patient Participation
5%
Keyphrases
TAB2
20%
6p25 Deletion
20%
Haploinsufficiency
18%
Ephrin Receptors
18%
Neurodevelopmental Disorders
18%
Parent-reported Outcomes
18%
Chromosomal Aberrations
18%
Chromosome 6
18%
Phenotypic Spectrum
18%
KCNQ5
6%
Influential Genes
6%
BAI3
6%
COL12A1
6%
Neurodevelopmental Phenotypes
6%
Bronchomalacia
6%
Akirin2
6%
