Though not diagnoses or conditions, Transgender & Gender-Diverse and Foster Care are included here to guide clinicians in addressing the numerous opportunities clinicians may have to improve outcomes for children and youth described by those terms.ge
Acute Flaccid Myelitis (AFM) Angelman Syndrome Anxiety Disorders Anxiety Disorders & Attention Deficit Hyperactivity Disorder (ADHD) Arginase Deficiency Asthma Attention-Deficit/Hyperactivity Disorder (ADHD) & Disruptive Behaviors Attention-Deficit/Hyperactivity Disorder (ADHD) & Mood Disorders Autism Spectrum Disorder Biotinidase Deficiency Bronchopulmonary Dysplasia Celiac Disease Cerebral Palsy Charcot-Marie-Tooth Disease (Hereditary Motor Sensory Neuropathy) Childhood Absence Epilepsy Congenital Diaphragmatic Hernia (CDH) Constipation Cornelia de Lange Syndrome Cranial Deformation & Craniosynostosis Cystic Fibrosis Depression Diagnosis Prevalence List Down Syndrome Duchenne & Becker Muscular Dystrophies Duchenne & Becker Muscular Dystrophies: Cardiomyopathy Fabry Disease Fetal Alcohol Spectrum Disorder Distinguished from Autism Fetal Alcohol Spectrum Disorders Foster Care Fragile X Syndrome Galactosemia Gastroesophageal Reflux Disease Headache (Migraine & Chronic) Hearing Loss & Deafness Homocystinuria (Classic) Infantile Spasms Inflammatory Bowel Disease Intellectual Disability & Global Developmental Delay LCHAD/TFP Deficiency Lennox-Gastaut Syndrome Leukodystrophies MCADD (Medium-Chain Acyl-CoA Dehydrogenase) Maple Syrup Urine Disease (MSUD) Mucopolysaccharidosis Type I & Motor Development Mucopolysaccharidosis Type I (MPS 1) Mucopolysaccharidosis Type I (MPS 1) Genetics Mucopolysaccharidosis Type I (MPS 1) Hematopoietic Stem Cell Transplantation & Enzyme Replacement Therapy Mucopolysaccharidosis Type I (MPS 1) Orthopedic Manifestations & Treatments Myotonic Muscular Dystrophy Type 1 Neurofibromatosis Type 1 Obesity in Children Obsessive-Compulsive Disorder (OCD) Other Names for Diagnoses & Conditions PKU & Pterin Defects Postural Orthostatic Tachycardia Syndrome (POTS) Prader-Willi Syndrome Prader-Willi Syndrome & Cognitive & Psychiatric Issues Prader-Willi Syndrome Genetics Prader-Willi Syndrome Nutrition & Diet Prader-Willi Syndrome and Complications from Obesity Premature Infant Follow-Up Premature Infant and Low Birthweight Premature Infant and Retinopathy of Prematurity Puberty & Pubertal Variations Rett Syndrome Seizures/Epilepsy Sickle Cell Disease Somatic Symptom Disorder & Functional Neurologic Disorders Spina Bifida Spinal Cord Injury Spinal Muscular Atrophy Substance Use Disorders Super Weird Condition Super Weird Condition Super Weird Condition Draft Tourette Syndrome Traumatic Brain Injury Tuberous Sclerosis Complex (TSC) Turner Syndrome Tyrosinemia Type 1 VLCADD XXY (Klinefelter) Syndrome 22q11.2 Deletion Syndrome
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Diagnosis Prevalence

Includes pediatric prevalence data for over 150 conditions and allows calculation of the number expected in a practice.