Medicine & Life Sciences
Phenotype
100%
Neonatal Screening
96%
Mucopolysaccharidosis I
94%
Hardikar syndrome
78%
Metabolomics
73%
Vitamin B 12
73%
Hartnup Disease
63%
Multiple Sulfatase Deficiency Disease
61%
Liver Transplantation
60%
Laryngeal cleft
60%
Riboflavin Deficiency
55%
Propionic Acidemia
53%
Methylmalonic acidemia
50%
Leigh Disease
49%
Multiple Hamartoma Syndrome
49%
Megaloblastic Anemia
48%
Sulfatases
48%
Glycogen Storage Disease Type II
47%
Osteopetrosis
47%
Thrombotic Microangiopathies
45%
Genetic Counseling
43%
Electron Transport
42%
Haploinsufficiency
42%
Riboflavin
41%
Rhabdomyolysis
41%
Electron Transport Complex IV
39%
Counselors
38%
Arteriovenous Malformations
38%
Intellectual Disability
36%
Transfer RNA
36%
Cell Transplantation
35%
Exome
35%
Pediatricians
34%
Regulator Genes
34%
Myelin Sheath
34%
Macrocytic Anemia
33%
Child
31%
Cysteine
31%
Seizures
30%
Early Diagnosis
29%
Enzymes
29%
Sulfur
29%
Glycosaminoglycans
26%
Genes
26%
Tensins
24%
Milrinone
24%
Hamartoma
23%
Neutropenia
22%
Language Development Disorders
22%
Chromosomes, Human, Pair 6
21%