| Members |
targetComponentId |
| 10-30% body burnt |
Burn any degree involving 10-19 percent of body surface |
| Forbrænding af over 10-30 % af legemsoverfladen |
Burn any degree involving 30-39 percent of body surface |
| 11-hydroxyetiocholanolon |
11-hydroxyandrosterone (substance) |
| 15 year examination |
Child 15 year examination (procedure) |
| Undersøgelse af barn - 15 år |
Child 15 year examination (procedure) |
| 15 year examination |
Child 15 year examination (procedure) |
| 16-dehydroprogesterone hydratase |
16-alpha-hydroxyprogesterone dehydratase |
| 17-beta-estriol |
Estradiol |
| måling af 18-hydroxydeoxycortisol |
18-Hydroxycortisol measurement |
| partiel trisomi 1q-syndrom |
Partial trisomy of long arm of chromosome 1 (disorder) |
| partiel trisomi 1q-syndrom |
Trisomy 1q is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the long arm of chromosome 1, with a highly variable phenotype principally characterized by intellectual disability, short stature, craniofacial dysmorphism (including macro/microcephaly, prominent forehead, posteriorly rotated, low-set ears, abnormal palpebral fissures, microphthalmia, broad, flat nasal bridge, high-arched palate, micro/retrognathia), cardiac defects and urogenital anomalies. Patients may also present cerebral (e.g. ventriculomegaly) and gastrointestinal malformations, as well as dystonic tremor and recurrent respiratory tract infections. |
| 2,2-dichloro-1,1-difluoroethylmethyl-ether |
Methoxyflurane |
| 2-Thio,4-Carboxythiazolidine |
2-sulfanylidene-1,3-thiazolidine-4-carboxylic acid |
| måling af 2-thio,4-carboxythiazolidin |
2-sulfanylidene-1,3-thiazolidine-4-carboxylic acid measurement (procedure) |
| 21q partial trisomy syndrome |
21q partial distal trisomy (disorder) |
| 21q partial trisomy syndrome |
21q partial trisomy (disorder) |
| 22q11 microdeletion with complete DiGeorge sequence |
A rare chromosomal anomaly which causes a congenital malformation disorder that is typically characterized by cardiac defects, palatal anomalies, facial dysmorphism, developmental delay and immune deficiency. |
| 24 hour urine volume (& level) |
24 hour urine volume - finding |
| 24 hour urine volume (& level) |
24 hour urine sample volume measurement |
| dyrehagl, størrelse 3 |
Shot size |
| dyrehagl, størrelse 3 |
Shotgun shot |
| 3 day faecal fat estimation (& level) |
3 day faecal fat estimation |
| 3,4 Methylhippurate |
Para-methyl hippurate (substance) |
| måling af 3,4-methylhippurat |
para-Methyl hippurate measurement (procedure) |
| 3-Hydroxybutylcarnitine |
3-hydroxybutyrylcarnitine (substance) |
| måling af 3-hydroxybutylcarnitin |
3-hydroxybutyrylcarnitine measurement |
| 3-tree-Pharmacia pollen mix |
Tree pollen (substance) |
| 3-tree-Pharmacia pollen mix allergen |
Tree pollen (substance) |
| 3/4-krone |
Crown |
| Forbrænding af 30-50 % af legemsoverfladen |
Burn any degree involving 40-49 percent of body surface |
| 30-50% body burnt |
Burn any degree involving 40-49 percent of body surface |
| 30-50% body burnt |
Burn any degree involving 30-39 percent of body surface |
| Forbrænding af 30-50 % af legemsoverfladen |
Burn any degree involving 50-59 percent of body surface |
| Forbrænding af 30-50 % af legemsoverfladen |
Burn any degree involving 30-39 percent of body surface |
| 30-50% body burnt |
Burn any degree involving 50-59 percent of body surface |
| dyrehagl, størrelse 4 |
Shotgun shot |
| dyrehagl, størrelse 4 |
Shot size |
| 4,5-Dihydroxyhexanolactone |
4,5-dihydroxyhexanoate (substance) |
| 4-Allylmethoxy-2-phenol |
Eugenol |
| 4-Hydroxyphenylpyruvate dioxygenase deficiency |
Hawkinsinuria (disorder) |
| 4-Hydroxyphenylpyruvate dioxygenase deficiency |
4-Hydroxyphenylpyruvate dioxygenase deficiency (disorder) |
| 4-Hydroxyphenylpyruvate dioxygenase deficiency |
Tyrosinemia type III (disorder) |
| overdosis af 4-quinoloner |
Quinolone antibacterial overdose |
| overdosis af 4-quinoloner, uvist med hvilken hensigt |
Quinolone antibacterial overdose |
| forgiftning med 4-quinoloner |
Fluoroquinolone poisoning (disorder) |
| forgiftning med 4-quinoloner, uvist med hvilken hensigt |
Fluoroquinolone poisoning (disorder) |
| 5-OH indole acetic acid (& level (& urine)) |
5-hydroxyindole acetic acid (substance) |
| 5-OH indole acetic acid (& level (& urine)) |
5-hydroxyindole acetic acid (substance) |
| 5-OH indole acetic acid (& level (& urine)) |
5-Hydroxyindoleacetic acid measurement, quantitative, urine |
| 5-chlor-2-methyl-4-isothiazolin-3-one og 2-methyl-4-isothiazolin-3-one kathon (3:1 i vand) |
2-methyl-4-isothiazolin-3-one |
| 5-chlor-2-methyl-4-isothiazolin-3-one og 2-methyl-4-isothiazolin-3-one kathon (3:1 i vand) |
5-chloro-2-methyl-4-isothiazolin-3-one (substance) |
| Forbrænding af 50-70 % af legemsoverfladen |
Burn any degree involving 70-79 percent of body surface |
| 50-70% body burnt |
Burn any degree involving 70-79 percent of body surface |
| 50-70% body burnt |
Burn any degree involving 60-69 percent of body surface |
| Forbrænding af 50-70 % af legemsoverfladen |
Burn any degree involving 60-69 percent of body surface |
| 50-70% body burnt |
Burn any degree involving 50-59 percent of body surface |
| Forbrænding af 50-70 % af legemsoverfladen |
Burn any degree involving 50-59 percent of body surface |
| 6 mm kuglekaliber |
Bullet |
| 6-grass Pharmacia pollen mix |
Grass pollen |
| 6-grass Pharmacia pollen mix allergen |
Grass pollen |
| 6,5 mm kuglekaliber |
Bullet |
| 60-80% of predicted peak flow rate (& expiratory) |
60 to 80 percent of predicted peak expiratory flow rate |
| 7 mm kuglekaliber |
Bullet |
| 7/8-krone |
Crown |
| 8 mm kuglekaliber |
Bullet |
| partiel trisomi 8p-syndrom |
Partial trisomy of short arm of chromosome 8 |
| partiel trisomi 8p-syndrom |
Trisomy 8p is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the short arm of chromosome 8, with highly variable phenotype ranging from no dysmorphic features and only mild intellectual disability to patients with severe developmental delay, neonatal hypotonia, short stature, profound intellectual disability, mild dysmorphic features (e.g. mild ptosis, hypertelorism, down-slanting palpebral fissures, broad nasal bridge, short, prominent philtrum, abnormal dentition) and structural brain abnormalities. Autism, epilepsy, and spastic paraplegia have also been reported. |
| 9 mm kuglekaliber |
Bullet |
| partiel monosomi 9p-syndrom |
Monosomy 9p is a rare chromosomal anomaly characterized by psychomotor developmental delay, facial dysmorphism (trigonocephaly, midface hypoplasia, upslanting palpebral fissures, dysplastic small ears, flat nasal bridge with anteverted nostrils and long philtrum, micrognathia, choanal atresia, short neck), single umbilical artery, omphalocele, inguinal or umbilical hernia, genital abnormalities (hypospadia, cryptorchidism), muscular hypotonia and scoliosis. |
| A |
Abdominal lymph node tumor invasion status A (tumor staging) |
| A |
Upper case Roman letter A (qualifier value) |
| A/B-dækningsbehov - kirurg/tandlæge |
Requires antibiotic coverage for dental procedure |
| A/B-dækningsbehov - kirurg/tandlæge |
Requires antibiotic coverage for surgical procedure (finding) |
| A/B cover need - surgery &/or dentist |
Requires antibiotic coverage for surgical procedure (finding) |
| A/B cover need - surgery &/or dentist |
Requires antibiotic coverage for surgical procedure (finding) |
| A/B cover need - surgery &/or dentist |
Requires antibiotic coverage for dental procedure |
| A/B cover need - surgery &/or dentist |
Requires antibiotic coverage for dental procedure |
| A/N U/S scan for ? abnormality |
Antenatal ultrasound scan for possible abnormality (procedure) |
| A/N U/S scan normal +? dates |
Antenatal ultrasound scan normal and possibly inconsistent with estimated date of delivery (finding) |
| A/N amnio. for ? chrom.abnorm. |
Amniocentesis for possible chromosomal abnormality (procedure) |
| A/N amnio. for ? neural tube |
Amniocentesis for possible neural tube defect (procedure) |
| AA amyloidosis |
Amyloid A amyloidosis (disorder) |
| ACE inhibitor-aggravated angioedema-urticaria (disorder) |
ACE inhibitor-aggravated angioedema |
| ACTH deficiency |
ACTH deficiency |
| ACTH deficiency |
Isolated corticotropin deficiency |
| AD-amyloidose |
Senile brain amyloidosis |
| AD-amyloidose |
Amyloidosis of skin |
| AIDS with Burkitt's tumor |
Burkitt lymphoma co-occurrent with human immunodeficiency virus infection (disorder) |
| aids med demyeliniserende sygdom i centralnervesystemet |
Central nervous system demyelinating disease with acquired immunodeficiency syndrome (disorder) |
| AIDS with Kaposi's sarcoma |
Kaposi's sarcoma with AIDS (acquired immunodeficiency syndrome) |
| AIDS with Nocardia infection |
Nocardiosis with acquired immunodeficiency syndrome (disorder) |
| AIDS with abnormal weight loss |
Abnormal weight loss associated with AIDS |
| AIDS with acquired hemolytic anemia |
Acquired haemolytic anaemia associated with AIDS |
| aids med akut endokardit |
Acute endocarditis with AIDS (acquired immunodeficiency syndrome) |
| aids med akut myokardit |
Myocarditis with acquired immunodeficiency syndrome (disorder) |
| AIDS with agranulocytosis |
Agranulocytosis with acquired immunodeficiency syndrome (disorder) |
| AIDS with anemia |
Anemia associated with AIDS |
| aids med aplastisk anæmi |
Aplastic anemia with AIDS (acquired immunodeficiency syndrome) |
| Aids med baggrundsretinopati |
Retinopathy with acquired immunodeficiency syndrome (disorder) |
| aids med bakteriel pneumoni |
Bacterial pneumonia with AIDS (acquired immunodeficiency syndrome) |
| Aids med blindhed |
Blindness with AIDS (acquired immunodeficiency syndrome) |
FHIR