Pediatrics and adolescent medicine
#
A
- Abdominal pain in children (evaluation of)
- Abdominal wall defects
- Abdominoschisis
- Abetalipoproteinemia
- Abetalipoproteinemia neuropathy
- Absence seizures
- Abusive head trauma in infants and young children
- Acne (vulgaris)
- Acne conglobata
- Acne excoriee des jeunes filles
- Acne fulminans
- Acne mechanica
- Acne vulgaris
- Acquired phimosis
- Acquired strabismus
- Acute asthma exacerbation in children
- Acute bronchial asthma
- Acute febrile mucocutaneous lymph node syndrome
- Acute headache in children (evaluation of)
- Acute laryngitis
- Acute lymphoblastic leukemia
- Acute otitis media
- Acute pharyngitis
- Acute varicella-zoster
- ADA deficiency
- Adamantinoma
- Adenosine deaminase deficiency
- Adenylate kinase-2 deficiency
- ADHD
- Adolescent health
- Adolescent idiopathic scoliosis
- Adolescent preventive counseling
- Adolescent type 2 diabetes
- Adrenogenital syndrome
- Adult congenital heart disease
- Adult hydrocele
- Adult osteochondritis dissecans
- Advanced maternal age
- Agammaglobulinemia
- Aganglionosis
- AIS
- AK2 deficiency
- Alcohol-related birth defects
- Alcohol-related neurodevelopmental disorder
- Aldrich syndrome
- ALL
- Allergic purpura
- Allergic vasculitis
- Alloimmune disease of the fetus
- Alport syndrome
- Alternating strabismus
- Amblyopia
- AN (anorexia nervosa)
- Anal incontinence (children)
- Anaphylactoid purpura
- Anaphylactoid vasculitis
- Anatomic penile abnormalities
- Anencephaly
- Anisometropic amblyopia
- Anorexia
- Anorexia nervosa
- Antibody deficiency
- Apolipoprotein B deficiency
- Appendicitis (evaluation of abdominal pain in children)
- Arachnodactyly
- ARBD
- Arboviral diseases, Zika
- ARND
- Artemis SCID
- Articular cartilage defects
- ASD
- Asthma in children
- Astigmatism
- Astigmia
- Athabascan SCID
- Attention deficit disorder
- Attention deficit hyperactivity disorder in children
- Attenuated WAS (XLT)
- Atypical genitalia
- Atypical genitalia in neonates
- Atypical pneumonia (non-COVID-19)
- Autism spectrum disorder
- Autosomal dominant Opitz GBBB syndrome
- Autosomal-recessive severe combined immunodeficiency
B
- BA
- Bacteraemia in children
- Bacterial laryngitis
- Bacteriuria (urinary tract infections in children)
- Bart syndrome
- Bassen-Kornzweig syndrome
- Battered baby syndrome
- Bedwetting
- Behavioral insomnias of childhood
- Benign extra-axial epithelial nonglial CNS tumor
- Benign familial neonatal epilepsy
- Benign joint hypermobility syndrome
- Benign neonatal seizures
- Beta-thalassemia
- Beta-thalassemia intermedia
- Beta-thalassemia major
- Beta-thalassemia minor
- Betalipoprotein deficiency disease
- Bilateral pitting edema
- Biliary atresia
- Biliary flow obstruction
- Binge eating
- Bipolar affective disorder
- Bipolar disorder in children
- BN
- BNS
- Bone-forming sarcoma
- Bourneville disease
- Bowed legs
- BPBP
- Brachial plexus birth injury
- Brachial plexus birth palsy
- Brain tumor (medulloblastoma)
- Bronchial asthma (acute asthma exacerbation in children)
- Bronchial asthma (children)
- Bulimia
- Bulimia nervosa
- Buried penis
C
- C-21-hydroxylase deficiency
- CAE (absence seizures)
- CAE (generalized seizures in children)
- Capillary hemangioma
- Care of premature baby
- CATCH22
- Cavernous hemangioma
- Cayler cardiofacial syndrome
- CBA
- CD3 deficiency
- CD45 deficiency
- CDH
- Cellular immunodeficiency
- Central osteosarcoma
- Cerebral palsy
- Cernunnos-XLF deficiency
- CF
- CGD
- Charcot Marie Tooth disease
- Charcot-Marie-Tooth disease
- CHD
- CHD (developmental dysplasia of the hip)
- CHD (tetralogy of Fallot)
- Check-up
- Chicken pox (acute varicella-zoster)
- Chickenpox (acute varicella-zoster)
- Child abuse
- Child undernutrition
- Childhood absence epilepsy (absence seizures)
- Childhood absence epilepsy (generalized seizures in children)
- Childhood depression
- Childhood obesity
- Childhood parasomnias
- Childhood type 2 diabetes
- Chlamydophila pneumoniae (atypical pneumonia)
- Chondromalacia of the larynx
- Chronic granulomatous disease
- Chronic granulomatous disease of childhood
- Chronic idiopathic jaundice
- Circadian rhythm disorders
- Classical 21-hydroxylase deficiency
- Classical Reye syndrome
- Clearance for sport
- Cleft lip and palate
- Closed spina bifida
- Clubfoot
- Clubfoot deformity
- CMT (Charcot-Marie-Tooth disease)
- CMT (congenital muscular torticollis)
- Cold
- Colic
- Colic in infancy
- Combined immunodeficiency
- Comedones
- Comitant strabismus
- Common cold
- Common gamma chain deficiency
- Common hereditary lysosomal storage diseases
- Common toxic plant ingestions
- Communicating hydrocele
- Cone dystrophy
- Confusional arousals (parasomnias in children)
- Congenital adrenal hyperplasia
- Congenital adrenocortical hyperplasia
- Congenital betalipoprotein deficiency syndrome
- Congenital dysplasia of the hip
- Congenital heart disease
- Congenital hip dysplasia
- Congenital laryngeal stridor
- Congenital megacolon
- Congenital muscular torticollis
- Congenital penile curvature
- Congenital phimosis
- Congenital spherocytic hemolytic anemia
- Congenital spherocytosis
- Congenital talipes equinovarus
- Congenital torticollis
- Conotruncal anomaly face syndrome
- Consecutive strabismus
- Constipation
- Constipation in children
- Constitutional delay
- Conventional osteosarcoma
- Cooley anemia
- Core autism
- Cot death
- Coxalgia fugax
- Coxitis serosa
- Coxsackievirus infection
- Craniopharyngeal duct tumor
- Craniopharyngioma
- Crib death
- Croup
- Cryptorchidism
- Cyanosis in the newborn (evaluation of)
- Cyanotic heart disease
- Cylinder power
- Cystic biliary atresia
- Cystic fibrosis
- Cystic fibrosis of the pancreas
- Cystitis (urinary tract infections in children)
D
- DDH
- Deep space neck infection
- Defect in tunica vaginalis of the scrotum
- Delayed growth
- Delayed puberty
- Delayed sleep phase disorder/syndrome (DSPD/DSPS)
- Dendritic cell histiocytosis
- Depression in adolescents
- Depression in children
- Depression in young people
- Deprivation amblyopia
- DeSanctis-Cacchione syndrome
- Developmental delay (Down syndrome)
- Developmental dysplasia of the hip
- Diabetes mellitus (Type 2 diabetes in children)
- Diabetes type 1
- Diaper dermatitis
- Diaper rash
- Differences of sex development
- Difficulty with defecation
- DiGeorge syndrome
- Diseases of the retina
- Disorders of infant feeding
- DJS
- DNA ligase IV deficiency
- Dolichostenomelia
- Doose syndrome
- Down syndrome
- Down syndrome (DS)
- Dravet syndrome
- Drug-induced acne
- DSD
- DSM-IV autism
- Dubin-Johnson syndrome
- Duchenne muscular dystrophy
- Dysmotility
- Dysodontogenic epithelial tumor
- Dysplastic pulmonary valve stenosis
- Dyssomnias in children
- Dysthymic disorder in adolescents
- Dysthymic disorder in children
E
- Early infantile epileptic encephalopathy with suppression burst
- Early puberty
- Eating disorder
- EB
- EB simplex (EBS)
- EBV infection
- Ectopic testis
- Eczema-thrombocytopenia-immunodeficiency syndrome
- Edematous malnutrition
- EDS
- EHBA
- Ehlers-Danlos syndrome
- Emotional abuse
- Encopresis
- Enterobiasis
- Enterovirus 71 infection
- Enterovirus D-68
- Enuresis
- Eosinophilic granuloma
- Epidermolysis bullosa
- Epilepsy (generalized seizures in children)
- Epilepsy in children
- Epilepsy with myoclonic absences
- Epilepsy with myoclonic-astatic (previously astatic seizures
- Epstein-Barr virus infection
- Equinovarus
- Equinovarus foot deformity
- Erb's palsy
- Erb-Duchenne paralysis
- Erythema infectiosum
- Erythroblastosis fetalis
- Esophageal atresia and tracheoesophageal fistula
- Esotropia
- ETD
- Eustachian tube dysfunction
- EV-D68
- Evaluation of abdominal pain in children
- Evaluation of acute headache in children
- Evaluation of cyanosis in the newborn
- Evaluation of fever in children
- Evaluation of gait disorders in children
- Evaluation of infantile dystonia
- Evaluation of learning difficulty and cognitive delay
- Evaluation of nausea and vomiting in children
- Evaluation of primary amenorrhea
- Evaluation of rash in children
- Evaluation of short stature
- Exanthem subitum
- Exomphalos
- Exotropia
- Extrahepatic biliary atresia
- Eyelid myoclonia with absences
F
- Fabry disease
- Factor VIII deficiency
- Faltering growth
- Familial conjugated hyperbilirubinemias (Dubin-Johnson syndrome)
- Familial homozygous hypobetalipoproteinemia
- Familial nephritis
- FAS
- FASD
- Fatal granulomatosis of childhood
- Febrile convulsions
- Febrile seizure
- Fecal incontinence in children
- Fecal soiling
- Fecal withholding
- Femoral torsion
- Fetal alcohol effects
- Fetal alcohol spectrum disorder
- Fetal alcohol syndrome
- Fever in children (evaluation of)
- Fibrocystic disease of the pancreas
- Fifth disease
- Form-deprivation amblyopia
- Functional fecal incontinence
- Functional megarectum
- Fungal laryngitis
G
- G6PD deficiency
- Gait abnormality
- Gait disorders in children (evaluation of)
- Gangioneuroma
- Ganglioneuroblastoma
- Gaucher disease
- GBS (group B streptococcal infection)
- GBS disease
- GBS infection
- Gene map locus Xp11.23-p11.22
- Generalized atrophic EB (GABEB)
- Generalized epilepsy
- Generalized seizures in children
- Generalized tonic-clonic seizures
- German measles
- GHD
- Giles Smith syndrome
- Gilles de la Tourette syndrome (Tourette syndrome)
- Glandular fever
- Glucose-6-phosphatase deficiency
- Glucose-6-phosphate dehydrogenase deficiency
- Glucose-6-phosphate translocase deficiency
- Gonadal dysgenesis
- Group B strep
- Group B streptococcal infection
- Growth deficiency
- Growth failure (failure to thrive)
- Growth hormone deficiency in children
- GSD I
H
- Hallopeau-Siemens (HS)
- Hand foot and mouth syndrome
- Hand Schuller Christian disease
- Hand-foot-and-mouth disease
- Hand-Schuller-Christian disease
- Hard or red measles
- Harelip
- Hashimoto-Pritzker disease
- Head lice
- Head louse
- Hemangioma
- Hemangioma of infancy
- Hemoglobin SC (HbSC) disease
- Hemolytic anemia (hereditary spherocytosis)
- Hemolytic disease of the fetus and newborn
- Hemophilia
- Hemorrhagic capillary toxicosis
- Henoch-Schonlein purpura
- Hepatorenal glycogenosis
- Hereditary hyperbilirubinemias
- Hereditary motor and sensory neuropathy
- Hereditary retinal dystrophy
- Hereditary spherocytosis
- Heritable disorders of connective tissue
- HFM disease
- HFMD
- Hidden penis
- High-grade central osteosarcoma
- Hirschsprung disease
- Histiocytosis X syndrome
- Histiocytosis, Langerhans cell
- HMSN
- Homozygous HbS condition
- HPS (pyloric stenosis)
- HS (hereditary spherocytosis)
- HSP
- Human herpes virus type 3 infection
- Human herpesvirus 4 infection
- Human herpesvirus type 6 (HHV-6)
- Human herpesvirus type 7 (HHV-7)
- Hydrocele
- Hydrocele of the spermatic cord
- Hyperkinetic movements (Tourette syndrome)
- Hyperkinetic syndrome
- Hypermobility
- Hyperphenylalaninemia
- Hypersomnolence
- Hypertrophic pyloric stenosis
- Hypertropia
- Hypogammaglobulinemia
- Hypomania
- Hypospadias
- Hypotonia
- Hypotropia
- Hypovolemia (volume depletion in children)
I
- ICD-11 autism
- Icterus neonatorum
- IDDM
- Idiopathic generalized epilepsy
- Idiopathic hypertrophic pyloric stenosis
- Idiopathic muscular torticollis
- Idiopathic scoliosis
- IgA vasculitis (Henoch-Schonlein purpura)
- IHPS
- IL-7 receptor alpha chain deficiency
- Ileal diverticulum
- Immune fetal hydrops
- Immune thrombocytopenia
- Immunodeficiency 2; IMD2
- Impetigo
- Impetigo contagiosa
- Incomitant strabismus
- Inconspicuous penis
- Infant care
- Infant colic
- Infantile colic
- Infantile dystonia (evaluation of)
- Infantile gastroesophageal reflux disease (GERD)
- Infantile hemangioma
- Infantile periarteritis nodosa
- Infantile spasms syndrome
- Infantile strabismus
- Infectious laryngitis
- Infectious mononucleosis
- Infectious pharyngitis
- Inflicted childhood neurotrauma
- Inflicted traumatic brain injury
- Infrequent defecation
- Infundibular pulmonary stenosis
- Inherited neuropathy
- Inherited retinal degeneration
- Insomnia (children)
- Insufficient sleep
- Insulin-dependent diabetes
- Intellectual disability
- Interatrial communications (atrial septal defects)
- Interleukin-7 receptor alpha chain deficiency
- Intermittent strabismus
- Intersex
- Intestinal malrotation
- Intoeing
- Intussusception
- Invagination of intestine
- Irritable hip
- Isolated biliary atresia
- ITP
J
- JA
- JAE (absence seizures)
- JAE (generalized seizures in children)
- JAK3 deficiency
- Janus kinase 3 deficiency
- Janz syndrome
- Jaundice in the newborn
- JCA
- Jeavons syndrome
- JIA
- JME (absence seizures)
- JME (generalized seizures in children)
- JRA
- Junctional EB (JEB)
- Juvenile absence epilepsy (absence seizures)
- Juvenile absence epilepsy (generalized seizures in children)
- Juvenile arthritis
- Juvenile chronic arthritis
- Juvenile diabetes
- Juvenile hemangioma
- Juvenile idiopathic arthritis
- Juvenile myoclonic epilepsy (absence seizures)
- Juvenile myoclonic epilepsy (generalized seizures in children)
- Juvenile osteochondritis dissecans
- Juvenile rheumatoid arthritis
K
L
- Langerhans cell granulomatosis
- Langerhans cell histiocytosis
- Laparoschisis
- Laryngitis
- Laryngomalacia
- Laryngotracheobronchitis
- Late pubertal development
- Late-onset congenital adrenal hyperplasia
- Late-onset idiopathic scoliosis
- Latent strabismus
- LCH
- Lead poisoning
- Lead toxicity
- Learning difficulty and cognitive delay (evaluation of)
- Legg-Calvé-Perthes disease
- Legionella pneumophila pneumonia
- Lennox-Gastaut syndrome (absence seizures)
- Lennox-Gastaut syndrome (generalized seizures in children)
- Letterer Siwe disease
- Letterer-Siwe disease
- Lice
- Limit-setting disorder
- Lipoid nephrosis (minimal change disease)
- Little League elbow
- Littre's hernia
- LM
- Louse
- LSDs
- Lysosomal storage disorders
M
- Major depressive disorder in adolescents
- Major depressive disorder in children
- Maladie de Roger
- Maldescended testis
- Malnutrition (failure to thrive)
- Malnutrition (kwashiorkor)
- Mamillaria
- Mania
- Manic depression (children)
- Manifest strabismus
- Marasmic-kwashiorkor
- Marfan syndrome
- Marfan's disease
- Measles infection
- Meckel diverticulum
- Meconium aspiration syndrome
- Meconium aspiration syndrome (MAS)
- Mediterranean anemia
- Medulloblastoma
- MEI
- Meningocele
- Meningomyelocele
- Mental retardation (Down syndrome)
- MFS
- Microcephaly, Zika virus
- Micropenis
- Microsomal triglyceride transfer protein deficiency
- Middle ear infection
- Midgut volvulus
- Migraine headache in children
- Miliaria
- Miliaria crystallina
- Miliaria profunda
- Miliaria pustulosa
- Miliaria rubra
- Minimal brain disorder
- Minimal change disease
- Miserable (malicious) malalignment syndrome
- Monocular strabismus
- Mononucleosis
- Morbilli
- Morgagni-Turner-Albright syndrome
- MPS disorders
- Mucocutaneous lymph node syndrome
- Mucopolysaccharidosis
- Mucoviscidosis
- Mucoviscidosis of the pancreas
- Mucovoidosis
- Mumps
- Muscular dystrophies
- Muscular torticollis
- Mycoplasma pneumoniae
- Myelomeningocele
- Myeloschisis
- Myoclonic epilepsy in infancy
N
- Napkin dermatitis
- Napkin rash
- Nappy dermatitis
- Nappy rash
- Nausea and vomiting in children (evaluation of)
- NBPP
- Neglect
- Neonatal brachial plexus palsy
- Neonatal jaundice
- Nephroblastoma
- Nephrosis
- Neural crest-derived tumors
- Neuroblastoma
- Neurogenic bowel disorder
- Newborn screening
- NF1
- NIDDM (Type 2 diabetes in children)
- Niemann-Pick disease type A
- Niemann-Pick disease type B
- Niemann-Pick disease type C
- Nightmare disorder (parasomnias in children)
- Nightmares (parasomnias in children)
- Nil disease
- Nits
- Nocturia
- Nocturnal enuresis
- Non-accidental brain injury
- Non-insulin-dependent diabetes mellitus (Type 2 diabetes in children)
- Non-retractile foreskin
- Nonclassical 21-hydroxylase deficiency
- Noncommunicating hydrocele
- Nonretractile foreskin
- Nonrotation
- Noonan syndrome
- NS
O
- Obesity in children
- Obesity, pediatric
- Observation hip
- Obstetric brachial plexopathy
- Obstetrical brachial plexus palsy
- Obstructive sleep apnea (OSA) in children
- Occupational acne
- OCD
- Ocular misalignment
- OD
- Ohtahara syndrome
- OME
- Omphalocele and gastroschisis
- Omphalomesenteric duct remnant
- Online Mendelian Inheritance in Man (OMIM) #301000
- Open spina bifida
- Organic fecal incontinence
- Orofacial cleft
- OSD
- Osgood-Schlatter disease
- Osteoblastic osteosarcoma
- Osteochondritis deformans
- Osteochondritis dissecans
- Osteochondritis of the hip
- Osteochondrosis
- Osteonecrosis
- Osteosarcoma
- Ostium secundum defect
- Otitis media with effusion
- Out-toeing
- Overdose in children
- Overflow incontinence
- Overvirilized female
- Oxyuriasis
P
- Paediatric type 2 diabetes
- PAH deficiency
- Pancreas fibrocystic disease
- Pancreatic cystic fibrosis
- Panhypogammaglobulinemia
- Panner disease
- Paraomphalocele
- Paraphimosis (anatomic penile abnormalities)
- Parasomnias in children
- Parotitis
- Partial FAS
- Partial fetal alcohol syndrome
- Parvor nocturnus
- Parvovirus
- Patent ductus arteriosus
- Patent processus vaginalis
- Pathologic phimosis
- PDA
- Pediatric depression
- Pediatric epilepsy
- Pediatric hydrocele
- Pediatric ingestions
- Pediatric MDD
- Pediatric migraine
- Pediatric obesity
- Pediatric overdose
- Pediatric sexual abuse
- Pediatric type 2 diabetes
- Pediatric UTI
- Pediculosis capitis
- Pelvic floor weakness
- Penile curvature
- Persistent crying
- Perthes disease
- Petit mal seizures
- Pharyngotympanic tube dysfunction
- Phenylalanine hydroxylase deficiency
- Phenylketonuria
- Physical abuse
- Physiologic phimosis
- PID (hypogammaglobulinemia)
- Pigeon toe
- Pigmentary retinal dystrophy
- Pigmentary retinopathy
- Pimples
- Pinworm infection
- PKU
- Plant poisoning
- Plumbism
- PNET
- PNET-MB
- PNP deficiency
- Poisonous plants
- Pompe disease
- Posterior fossa PNET
- Postnatal biliary atresia
- Postural deformity
- Postural torticollis
- Prader-Willi syndrome
- Precocious puberty
- Precocity
- Premature newborn care
- Preventive care
- Preventive visit
- Prickly heat
- Primary amenorrhea (evaluation of)
- Primary antibody deficiency
- Primary immune thrombocytopenia
- Primary immunodeficiency (hypogammaglobulinemia)
- Primary immunodeficiency (SCID)
- Primary strabismus
- Primitive neuroectodermal tumor
- Progressive septic granulomatosis
- PS
- Pseudohermaphrodite
- Pseudorubella
- Pubertal delay
- Puberty
- Pulmonary stenosis
- Pulmonary valve dysplasia
- Pulmonary valve stenosis
- Purine nucleoside phosphorylase deficiency
- PWS
- Pyelonephritis
- Pyknolepsy
- Pyloric stenosis
- Pyoderma
R
- RAG1 deficiency
- RAG2 deficiency
- Rash in children (evaluation of)
- Rathke's pouch tumor
- RBD
- Recessive dystrophic EB (RDEB)
- Recombination activating gene 1 deficiency
- Recombination activating gene 2 deficiency
- Recurrent isolated sleep paralysis
- Recurrent pediatric headache
- Recurrent strabismus
- REM sleep behavior disorder
- Respiratory syncytial virus (infection)
- Respiratory syncytial virus infection
- Reticular dysgenesis (SCID)
- Retina tumor
- Retinal degeneration
- Retinal disease
- Retinal dystrophy
- Retinitis pigmentosa
- Retinoblastoma
- Retropharyngeal abscess
- Reye syndrome
- Reye's syndrome
- Reye's-like syndrome
- Reye-like syndrome
- Rh incompatibility
- Rhesus D disease
- Rheumatoid purpura
- Rickets
- Right ventricular outflow obstruction
- Rod dystrophy
- Rod/cone dystrophy
- Roseola
- Roseola infantum
- RPA
- RSV (respiratory syncytial virus)
- Rubella
- Rubeola
S
- Salt waster
- SBS (abusive head trauma in infants)
- Scarlatina
- Scarlet fever
- SCFE
- School sores
- Scrotal fluid collection
- Secondary antibody deficiency
- Secondary immunodeficiency
- Secondary phimosis
- Secondary strabismus
- Sepsis in children
- Serous otitis media
- Severe combined immunodeficiency
- Severe malnutrition
- Severe myoclonic epilepsy in infancy
- Sex reversal
- Sexual abuse and assault
- Shaken baby syndrome
- Shaken impact syndrome
- Shaken infant syndrome
- Shock (volume depletion in adults)
- Short stature (evaluation of)
- Shprintzen syndrome
- Sickle cell anemia
- Sickle cell disease (SCD)
- Sickle cell hemoglobinopathies
- SIDS
- Simple hydrocele
- Simple virilizer
- Sinus venosus defect
- Sixth disease
- Slapped cheek disease
- Sleep drunkenness (parasomnias in children)
- Sleep terrors (parasomnias in children)
- Sleep-disordered breathing (dyssomnias in children)
- Sleep-onset association disorder
- Sleepwalking (parasomnias in children)
- Slipped capital femoral epiphysis
- Somnambulism (parasomnias in children)
- Sore throat (pharyngitis)
- Sore throat (tonsillitis)
- Spastic diplegia
- Spina bifida and neural tube defects
- Spina bifida aperta
- Spina bifida cystica
- Spina bifida occulta
- Spinal dysraphism
- Sports preparticipation physical
- Squint
- Stomach flu
- Strabismic amblyopia
- Strabismus
- Strawberry nevus
- Strep group B
- Strep throat
- Streptococcus agalactiae
- Stunting
- Sudamina
- Sudden infant death syndrome
- Superficial Staphylococcus skin infection
- Superficial Streptococcus skin infection
- Supravalvar pulmonary stenosis
T
- T1DM
- T2DM
- T2DM in children
- Talipes equinovarus
- Tay-Sachs disease
- Teenage type 2 diabetes
- TEF
- Tetralogy of Fallot
- Threadworm infection (pinworm)
- Three-day fever
- Thrombocytopenic purpura
- Tibial torsion
- Tibial tubercle traction apophysitis
- Tic (Tourette syndrome)
- Tic disorder (Tourette syndrome)
- Tics (Tourette syndrome)
- TOF
- Tonic-clonic seizures
- Tonsillitis
- Tonsillopharyngitis (pharyngitis)
- Tonsillopharyngitis (tonsillitis)
- Topical anhidrotic asthenia
- Torsion of the lower limb in children
- Torsional strabismus
- Tourette
- Tourette disorder (Tourette syndrome)
- Tourette syndrome
- Toxic ingestions in children
- Toxic synovitis
- Tracheoesophageal atresia
- Transient synovitis of the hip
- Trapped penis
- Trisomy 21
- True hermaphrodite
- TS
- TS (Tourette syndrome)
- TSC
- Tuberous sclerosis
- Tuberous sclerosis complex
- Turner syndrome
- Type 1 diabetes
- Type 1 diabetes mellitus
- Type 1 glycogenosis
- Type 1 neurofibromatosis
- Type 2 diabetes in adolescents
- Type 2 diabetes in children
- Type 2 diabetes in teenagers
- Type I glycogen storage disease
- Type I GSD
- Type II diabetes mellitus (children)
U
- Undervirilized male
- Underweight
- Undescended testicle(s)
- Undescended testis
- Unroofed coronary sinus
- Urinary tract infections in children
- UTI (Urinary tract infections in children)
V
- Valvar pulmonary stenosis
- Varicella
- Varicella zoster
- Varicella-zoster virus infection
- Vasculitis (Kawasaki disease)
- Velocardiofacial syndrome
- Ventricular septal defects
- Vesicular stomatitis with exanthem
- Viral gastroenteritis in children
- Viral laryngitis
- Vit D deficiency
- Vitamin D deficiency
- Vitamin D dysregulation
- Vitamin D insufficiency
- Vitelline duct remnant
- Voiding dysfunction
- Volume depletion in children
- Von Gierke disease
- von Recklinghausen disease
- VSD
W
- Waiter's tip deformity
- WAS-related disorders
- Weber-Cockayne EB
- Well baby care
- Well-baby care
- Well-child care
- Well-child visit
- Werlhof disease
- West syndrome
- West syndrome (generalized seizures)
- Wilms tumor
- Wiskott-Aldrich syndrome
X
- X-linked congenital neutropenia (XLN)
- X-linked recessive immunodeficiency
- X-linked severe combined immunodeficiency
- X-linked thrombocytopenia (XLT)
- Xeroderma pigmentosum
- XP
Z
A
- Abdominal pain in children (evaluation of)
- Abusive head trauma in infants and young children
- Acute asthma exacerbation in children
- Acute bronchial asthma
- Acute headache in children (evaluation of)
- Acute pharyngitis
- Alloimmune disease of the fetus
- Appendicitis (evaluation of abdominal pain in children)
- Atypical pneumonia (non-COVID-19)
B
- Bacteraemia in children
- Battered baby syndrome
- Benign familial neonatal epilepsy
- Benign neonatal seizures
- BNS
- Bronchial asthma (acute asthma exacerbation in children)
C
- CAE (generalized seizures in children)
- Child abuse
- Childhood absence epilepsy (generalized seizures in children)
- Chlamydophila pneumoniae (atypical pneumonia)
- Classical Reye syndrome
- Cold
- Common cold
- Common toxic plant ingestions
- Cot death
- Crib death
- Croup
D
E
- Early infantile epileptic encephalopathy with suppression burst
- Emotional abuse
- Epilepsy (generalized seizures in children)
- Epilepsy in children
- Epilepsy with myoclonic absences
- Epilepsy with myoclonic-astatic (previously astatic seizures
- Erythroblastosis fetalis
- Evaluation of abdominal pain in children
- Evaluation of acute headache in children
- Eyelid myoclonia with absences
F
G
H
- Hemolytic disease of the fetus and newborn
- HPS (pyloric stenosis)
- Hypertrophic pyloric stenosis
- Hypovolemia (volume depletion in children)
I
- Idiopathic hypertrophic pyloric stenosis
- IHPS
- Immune fetal hydrops
- Infectious pharyngitis
- Inflicted childhood neurotrauma
- Inflicted traumatic brain injury
- Intussusception
- Invagination of intestine
J
- JAE (generalized seizures in children)
- Janz syndrome
- Jeavons syndrome
- JME (generalized seizures in children)
- Juvenile absence epilepsy (generalized seizures in children)
- Juvenile myoclonic epilepsy (generalized seizures in children)
L
- Laryngotracheobronchitis
- Lead poisoning
- Lead toxicity
- Legionella pneumophila pneumonia
- Lennox-Gastaut syndrome (generalized seizures in children)
M
N
O
P
- Pediatric epilepsy
- Pediatric ingestions
- Pediatric overdose
- Pediatric sexual abuse
- Physical abuse
- Plant poisoning
- Plumbism
- Poisonous plants
- Pyloric stenosis
R
- Respiratory syncytial virus (infection)
- Respiratory syncytial virus infection
- Retropharyngeal abscess
- Reye syndrome
- Reye's syndrome
- Reye's-like syndrome
- Reye-like syndrome
- Rh incompatibility
- Rhesus D disease
- RPA
- RSV (respiratory syncytial virus)
S
- SBS (abusive head trauma in infants)
- Sepsis in children
- Severe myoclonic epilepsy in infancy
- Sexual abuse and assault
- Shaken baby syndrome
- Shaken impact syndrome
- Shaken infant syndrome
- Shock (volume depletion in adults)
- SIDS
- Sore throat (pharyngitis)
- Stomach flu
- Strep throat
- Sudden infant death syndrome