Ehrlichiosis
Amino acid metabolic disease
Streptococcus group A infection
Austin type infantile cerebral thioliposis
Whooping cough
Brazilian purple fever
Depilatory mania
Viral myocarditis
Bladder valgus
Fulminant dysentery
Streptococcus group B infection
Phenylketonuria
rickets
Insect plot
Autosomal recessive cerebral arteriopathy and arteriosclerosis with subcortical infarction and leukoencephalopathy
Puncturing abscess head folliculitis and perifolliculitis
Chiyoudan
CM1 ganglioside storage disease
Intestinal gram negative bacilli meningitis
Ugly fetus
Kawasaki disease
Enteropathogenic Escherichia coli infection
asthmatoid bronchitis
Globus pallidus nigra erythronuclear pigmented degeneration
Protein heat dystrophy
Dansha
DOPA reactive dystonia
Digoorg syndrome
iodine deficiency
Patent ductus arteriosus
Massive amniotic fluid inhalation
Childhood autism
Pancreatic insufficiency with neutropenia syndrome in children
Sleep disorders in children
Children's social phobia
Childhood hyperactivity syndrome
Children with learning disabilities
Child anxiety disorder
Tic Disorder
Childhood emotional disorder
Abdominal pain in children
Child health
Stuttering in children
Childhood leukemia
Child phobia
Acute benign myositis in children
Sinusitis in children
Seizures and epilepsy syndrome
Pulmonary cystic fibrosis
Abdominal fissure
Tetralogy of Fallot
Pneumococcal meningitis
Anal atresia
Osteochondrosis
Calcaneal epiphysis
Concomitant strabismus
Hyperimmunoglobulin E syndrome
Bone lengthening
Fibrous dysplasia of bone
Ectopic origin of coronary artery
Mixed renal tubular acidosis
Annular pancreas
Respiratory syncytial virus pneumonia
Acute disseminated encephalomyelitis
Chicken breast
Cytomegalovirus infection
Pseudoaldosteronism
Giant
Scoliosis
Spastic cerebral palsy
Mental retardation
Cytomegalovirus disease
Familial Mediterranean fever
Familial anti vitamin D rickets
convulsions
Proximal tubular acidosis
Giant fetus
Progressive muscular dystrophy
Tuberous sclerosis
Coramine poisoning
Kartagener syndrome
Quinine poisoning
Cretinism
Antibody immunodeficiency disease
Cranial stenosis
Mumps
Riley day syndrome
Letrell civir disease
Combined immunodeficiency disease
Horse tooth
Immune deficiency disease
Molars
Fontanelle dysplasia
maternofetal blood group incompatibility
Breast milk jaundice
Ringworm of milk
Cerebral palsy syndrome
Encephalocele and meningocele
Pustulosis
Encephalocele
Milk hemp
Niznov's syndrome
O-leg
Conduct disorder
Alligator skin infant syndrome
spleen gan disease
Umbilical hernia
Air hernia
Omphalitis
Hypoxic ischemic encephalopathy
Omphalocele megatongue megasoma syndrome
Chikungunya virus disease
Affective cross leg rubbing
Umbilical mesenteric duct polyp
milk aspiration pneumonia
Hemolytic uremic syndrome
Mentally retarded
Rh blood group incompatibility
amblyopia
Rotor syndrome
Schumann's disease
Esophageal duplication
Neurospinous erythrocytosis
Neuronal ceroid lipofuscinosis
Hernia
Retinoblastoma
Mumps
Sha Zi
Steele's disease
Neuroendocrine tumor
Congenital absence, atresia and stenosis of duodenum
Upper airway obstruction
Salicylic acid poisoning
Renal hypoplasia
Hand foot mouth disease
Varicella keratitis
Idiopathic hypercalciuria
Aspartyl glucosaminuria
Meconium constipation
Meconium aspiration syndrome
Glycogen accumulation disease
Glycogen storage disease type I
Glycogen storage disease type V
Fetal alcohol syndrome
Phagocytosis deficiency disease
Aerophagia
Glycogen storage disease type II
Vitamin A deficiency neuropathy
Trace element disorder
Rhabdomyosarcoma of vulva
Vitamin K deficiency disease
Vitamin dystrophy
Five late
Vitamin E deficiency neuropathy
Excessive intake of vitamin A
Viscott Aldrich syndrome
Five hard
Vitamin E deficiency
Vitamin D dependent rickets
Vitamin D deficiency rickets
Pinworm disease of vulva
Corneal ulcer caused by vitamin A deficiency
Vitamin D deficiency hand foot convulsion
Five soft
vitamin D intoxication
Pediatric hypochloric azotemia syndrome
Allergic purpura in children
Neonatal gastrointestinal duplication
Neonatal hepatitis B
Pediatric primary nephrotic syndrome
infantile convulsion
Fragile X chromosome in children
Pediatric hernia
Polio Guillain Barre syndrome
Children's white matter spongiform degeneration syndrome
Infantile myocarditis
Pediatric intracranial tumors
Thyroid diseases in children
Pediatric neurocutaneous syndrome
Hemolysis of newborn
Intraspinal tumor in children
Neonatal traumatic diseases
Amsterdam type dwarfism in children
Infantile dyspepsia
Chronic lymphocytic thyroiditis in children
Infantile endemic cretinism
Pediatric ventricular tachycardia
Congenital ovarian dysplasia, Turner's syndrome
Childhood diabetes mellitus
Connective tissue disease in children
Pediatric dwarfism retinal atrophy deafness syndrome
Herpetic angina in children
Congenital leukocyte granulosa syndrome
Hydronephrosis in children
Pediatric hyperviscosity syndrome
Infantile propionic acidemia
Congenital muscular torticollis
Children's deformity
Congenital talipes equinovarus
Pediatric angioimmunoblastic lymphadenopathy