SLO domain: Paediatrics, clinical picture
accidents, poisonings, emergencies
2000
cardiovascular disorders diseases and malformations of kidneys and urinary tract diseases of the endocrine organs gastrointestinal disorders growth and pubertal disturbances haemato-oncologic disorders immunological and allergic disorders infectious diseases metabolic disorders neonatology neurological disorders orthopedic disorders pathologies during pregnancy with consequences on the newborn psychiatry of childhood and adolescence respiratory disorders skin diseases
2016 ventricular septal defect [C IM 217]
6/0/0a
2017 congenital complete heart block
0/1/0a
2018 supraventricular tachycardia in children
0/0/0a
2019 heart murmur, innocent
4/0/1a
2020 rheumatic fever [C IM 44]
0/0/1a
2021 cardiomyopathy [C IM 218]
1/0/3a
2022 tetralogy / pentalogy of Fallot
6/0/1a
2023 hypertension in children
0/0/0a
2024 atrial septal defect [C IM 216]
5/0/2a
2025 coarctation of aorta, congenital
5/1/1a
2026 pulmonary stenosis (obstruction to right ventricular outflow) in children
4/2/0a
2027 ductus arteriosus, persistent
6/1/1a
2028 transposition of great arteries in infants
6/0/1a
2029
2030 hymen, imperforate, in children
1/1/1a
2032 adhesions of labia
0/3/1a
2033 urolithiasis / renal colic in children
1/0/2a
2034 urethral valves (malformation)
2/2/2a
2035 vesicourethric reflux [C SU 210]
2/2/1a
2037 hydronephrosis
3/1/0a
2038 enuresis, primary / secondary
0/2/0a
2039 renal failure, acute / chronic in children
3/1/1a
2040 Fanconi syndrome (kidney)
0/0/0a
2043 glomerulonephritis in children
0/3/0a
2044 hemolytic uraemic syndrome
0/1/0a
2045 nephrotic syndrome in children
2/1/1a
2046 adreno-cortical failure in children
2/1/0a
2047 Cushing's syndrome or hypercortisolism [C IM 81, C SU 227]
0/1/0a
2048 adrenogenital syndrome
1/3/1a
2049 cryptorchidism, undescended testis [C SU 212]
2/1/1a
2051 hypothyroidism, neonatal and infantile
2/4/4a
2052 diabetes mellitus type I / type II in children
4/1/0a
2053 diabetes insipidus [C IM 82]
1/0/1a
2054 pituitary failure [C IM 97]
2/3/1a
2055
2057 milk protein intolerance in children
2/2/2a
2058 celiac disease [C IM 274]
1/2/2a
2059 anal fissures [ C IM 290, C SU 157, C DE 79]
0/2/0a
2060 Meckel's diverticulum [C SU 146]
0/2/1a
2061 hernia, inguinal in children
4/0/0a
2062 hiatal hernia in children
2/1/3a
2063 Hirschsprung's disease (megacolon, congenital) [C SU 151]
1/2/0a
2064 constipation in children
0/1/3a
2065 pyloric stenosis, congenital
3/1/2a
2066 gynaecomastia in puberty
0/1/2a
2067 growth disorder, short stature / tall stature
7/0/1a
2069 Turner syndrome , gonadal dysgenesis [C GO 37]
5/1/3a
2070 Klinefelter syndrome
0/3/3a
2071 Marfan syndrome [C IM 20]
1/0/2a
2072 failure to thrive in children
6/0/3a
2073 obesity [C IM 101]
2/2/1a
2074 premature thelarche / pubarche
3/1/0a
2075 menstrual cycle, dysfunction in adolescence
2/2/0a
2076 puberty, precocious / delayed
5/1/1a
2154 genitalia, ambigous, mixed gonadal dysgenesis [C GO 36]
2/0/0a
2078 neuroblastoma
0/1/1a
2079 sarcoma of soft tissue including rhabdomyosarcoma [C SU 20]
0/0/0a
2080 nephroblastoma
0/0/0a
2081 lymphomas (Hodkin's / non-Hodgkin) [C IM 68]
4/1/0a
2082 leukemia, acute [C IM 69]
2/0/1a
2084 purpura, thrombocytopenic idiopathic
1/2/0a
2085 haemoglobinopathies [C IM 66]
2/0/0a
2086 anemia from iron deficiency [C IM 60]
1/0/0a
2087 aplastic / hypoplastic anaemia
2/0/0a
2088
2089 hypogammaglobulinaemia / agammaglobulinaemia
0/0/0a
2090 immunodeficiency syndromes
1/0/1a
2094 Kawasaki syndrome (mucocutaneous lymph node syndrome)
1/0/0a
2095 AIDS in children
1/0/0a
2096 rhino-conjunctivitis, allergic / rhinosinusitis, allergic [C OT 34]
5/1/0a
2097 purpura, Henoch-Schönlein (subgroup of hypersensitivity vasculitides) [C IM 42, C DE 38]
1/1/1a
2098 lupus erythematosus systemic [C IM 56]
0/0/2a
2099 arthritis, juvenile chronic [C IM 5]
1/0/0a
2101
2102 otitis media, acute, viral / bacterial [C OT 10]
1/1/0a
2103 impetigo [C DE 9]
1/0/0a
2104 upper respiratory tract infections
2/0/0a
2106 rhinitis, rhinosinusitis, acute [C OT 33]
1/3/0a
2107 stomatitis, herpetic [C IM 258, C OT 47]
0/0/0a
2108 meningococcaemia
3/2/0a
2109 pneumonia, community acquired, in children
7/2/1a
2110 colitis / enterocolitis / gastroenteritis infectious [C IM 275]
3/1/2a
2111 urinary tract infections (cystis, urethritis) in children
5/2/0a
2112 vulvovaginitis in children
0/1/1a
2113 orchitis /epididymitis
0/1/1a
2114 arthritis, septic / arthritis, reactive in children
2/1/0a
2115 brain abscess [C IM 147]
0/2/1a
2116 measles
2/0/2a
2117 rubella
4/0/0a
2118 varicella / herpes zoster [C IM 350, C DE 3]
4/0/1a
2119 exanthema subitum (roseola)
1/0/2a
2120 lymphangitis, acute / lymphadenitis, acute [C IM 353, C SU 122, C DE 84]
0/0/0a
2121 scarlet fever [C OT 57]
1/0/0a
2122 orbit, inflammation of / orbital cellulitis [C OP 52]
0/0/1a
2123 bacteraemia
2/3/2a
2124 mumps (epidemic parotits) [C OT 73]
1/0/1a
2125 mononucleosis infections [C IM 351, C OT 54]
1/0/1a
2126 whooping cough
5/0/0a
2127 diphtheria, including diphteric croup [C OT 53]
2/1/0a
2128 tetanus [C IM 357, C SU 6]
0/0/0a
2129 poliomyelitis [C IM 371]
0/0/1a
2130 tracheitis, acute / chronic [C IM 255, C OT 94]
1/0/1a
2131 viral croup (pseudocroup, laryngitis subglottica) [C OT 95]
4/0/1a
2132 peritonsillar abscess / retropharyngeal abscess [C OT 59]
1/0/1a
2133 bronchiolitis
4/1/0a
2134 erythema infectiosum, fifth disease (Ringenlroteln, mégalérythème épidermique)
1/0/1a
2250 balanitis
0/1/0a
2251 otitis media, chronic, with effusion (glue ear) / with central perforation of tympanic membrane [C OT 11]
1/0/0a
2252 mastoid abscess / purulent otomastoiditis [C OT 13]
1/0/0a
2253 otitis, external [C OT 5]
0/0/0a
2254 rhinitis, rhinosinusitis, chronic [C OT 35]
1/0/1a
2245 candidiasis, mouth / throat (thrush) [C IM 257, C SU 30, C OT 46]
0/1/0a
2135
2136 hyperglycaemia in childhood
4/1/0a
2137 rickets
1/0/2a
2140 dehydration in children
5/2/2a
2141 hypocalcaemia in neonates and children
0/1/1a
2144
2145 congenital dislocation of the hip
2/2/1a
2146 apnea in infant
2/3/3a
2147 meconium aspiration
5/2/1a
2148 perinatal asphyxia
4/1/2a
2149 birth injuries, common
2/0/1a
2150 congenital torticollis
2/1/2a
2151 congenital foot deformity [C IM 41, C SU 252]
1/1/1a
2152 epispadia / hypospadia [C SU 214]
2/0/0a
2153 hyaline membrane disease in newborn
5/2/2a
2155 neonatal pneumonia
4/4/4a
2156 cleft lip, jaw, palate [C SU 42, C OT 67]
2/0/0a
2157 postmature infant
1/0/2a
2159 hydrocephalus in newborn and cerebral malformations [C SU 28]
1/0/1a
2160 cataract in children
7/0/0a
2161 respiratory distress in infants
5/3/0a
2162 congenital malformations of kidney / of ureter / of urethra [C SU 201]
3/0/1a
2163 meconium ileus
2/2/1a
2164 enterocolitis, necroziting in infants
3/1/0a
2167 seizures in neonates
1/3/2a
2168 omphalocoele
2/0/0a
2169 volvulus of small intestine, congenital malrotation [C SU 145]
4/2/0a
2170 diaphragmatic hernia of the newborn
3/5/2a
2171 atresia in newbord (esophageal, intestinal, biliary, anal)
4/2/1a
2174 mongolian spot
1/0/0a
2175 milia in infants
1/0/0a
2176 erythema toxicum in infants
1/0/0a
2178 haemorrhagic disease of the newborn
3/0/0a
2179 neonatal meningitis
4/1/1a
2180 sepsis in neonates
6/1/2a
2181 conjunctivitis in newborn
1/1/0a
2185 macrosomia in neonates
2/1/2a
2186 infant, small for gestational age
5/1/0a
2187 prematurity in infants
4/1/4a
2188 rhesus/ ABO incompatibility
3/0/0a
2190 headache, migraine in children
0/2/0a
2191 retinoblastoma in children and adults [C OP 39]
0/1/0a
2192 cerebral palsy [C IM 119]
0/0/1a
2193 seizures, partial / generalized in children
1/1/0a
2194 spasms, infantile
0/1/3a
2195 absence attacks, typical, in children
1/1/0a
2196 neurofibromatosis (Recklinghausen's disease) [C IM 160, C DE 43]
0/0/0a
2197 spinal muscular atrophy
0/0/2a
2199 brain tumors, begign / malignant [C SU 27]
1/2/1a
2200 myopathy
0/0/2a
2201
2202 osteosarcoma
1/2/0a
2203 synovitis of hip, transient
1/1/0a
2205 spinal deformation (kyphosis, scoliosis, lordosis, including juvenile kyphosis = Scheuermann's disease) [C IM 47, C SU 58]
3/3/0a
2206 craniosynostosis in infants
1/1/0a
2207 osteogenesis imperfecta [C IM 22]
2/0/0a
2208 achondroplasia [C IM 1]
1/2/1a
2209 Ewing sarcoma
2/0/1a
2215 oligohydramnios [C GO 54]
3/1/1a
2249 hydramnios [C GO 53]
2/1/2a
2217 psychoses of the child and adolescent [C PS 14]
1/1/1a
2219 somnambulism, night terrors and nightmares (parasomnia) [C IM 186, C PS 67]
0/0/0a
2220 autism [C PS 2]
3/0/2a
2221 psychosomatic disorders (non specific symptoms:abdominal pain, headache, fatigue) [C PS 15]
3/3/0a
2222 encopresis [C PS 11]
0/0/0a
2223 tic disorders [C PS 5]
0/0/1a
2224 eating disorders in childhood [C PS 10]
2/0/1a
2225 mutism [C PS 13]
1/0/1a
2226 speech and laguage disorders in childhood, including stuttering [C PS 17]
1/0/0a
2227 psychic reaction to chronic disease [C PS 6]
0/1/3a
2228 depression in children [C PS 7]
3/1/0a
2230 dyslexia [C PS 9]
0/1/0a
2231 attention deficit hyperactivity disorder (ADHD, ADHS) [C PS 1]
1/1/1a
2232 psychic reaction to parental divorce [C PS 8]
0/0/0a
2233 parent - child relationship, disorders
4/1/1a
2234
2235 bronchopulmonary dysplasia
4/2/1a
2237 bronchial asthma acute / chronic [C IM 232]
5/0/2a
2238 adenoidal and tonsillar hypertrophy
1/2/1a
2239
2240 urticaria [C DE 37]
1/4/1a
2241 acne , hydradenitis suppurativa [C DE 53]
0/0/1a
2242 haemangioma of skin
1/1/0a
2243 seborrheic dermatitis in children
0/0/1a
2244 atopic / constitutional eczema [C DE 29]
2/2/2a
2246 pediculosis capitis and pubis [C DE 16]
0/0/0a
2247 scabies [C DE 17]
0/0/1a