Medicine & Life Sciences
Osteogenesis Imperfecta
100%
Phenotype
73%
Genes
47%
Mutation
40%
Intellectual Disability
39%
Undiagnosed Diseases
37%
Exome
34%
Whole Exome Sequencing
32%
Type 3 Osteogenesis imperfecta
29%
Neurodevelopmental Disorders
28%
Muscle Hypotonia
27%
Type IV Osteogenesis Imperfecta
26%
Attention Deficit Disorder with Hyperactivity
26%
Leukoencephalopathies
22%
Fibroblasts
21%
Genetic Databases
20%
Steroidogenic Factor 1
19%
Single Nucleotide Polymorphism
18%
Congenital Disorders of Glycosylation
18%
Proteins
17%
Human Genetics
17%
Tooth
17%
Child
16%
Sudden Cardiac Death
16%
Sexual Development
16%
Cataract Hutterite type
16%
Craniosynostoses
16%
RNA Splice Sites
16%
Brain Diseases
16%
dipalmitoleoylphosphatidylethanolamine
15%
Craniosynostosis, anal anomalies, and porokeratosis
15%
Autosomal Dominant Multiple Pterygium Syndrome
15%
Missense Mutation
15%
Strudwick syndrome
15%
Cataract
15%
White Matter
14%
Corner Fracture Type Spondylometaphyseal Dysplasia
14%
Crohn Disease
14%
Patient Reported Outcome Measures
14%
Human Development
13%
Noonan Syndrome 2
13%
fucokinase
13%
Catel Manzke syndrome
13%
proteasome maturation protein
13%
Megalencephaly
13%
Hormones
13%
Genome
13%
Haploinsufficiency
13%
Molecular Biology
13%