| Members |
targetComponentId |
| Auditory/vestibular test normal (& [hearing] or [audiogram]) |
Auditory/vestibular test normal (finding) |
| Auditory/vestibular test normal (& [hearing] or [audiogram]) |
Audiogram normal |
| Auditory/vestibular test normal (& [hearing] or [audiogram]) |
Hearing test normal |
| Augmentation - action |
Surgical augmentation - action |
| augmentationsgenioplastik vha. graft og implantat |
Augmentation of chin using sliding osteotomy and interpositional autograft (procedure) |
| augmentationsgenioplastik vha. graft og implantat |
Augmentation of chin using implant (procedure) |
| aurantimonasarter |
Genus Aurantimonas (organism) |
| Auscultation - action |
A listening to spontaneously generated body sounds |
| Auscultation - action |
Auscultation - action |
| Australian echidna |
Family Tachyglossidae (organism) |
| Australian echidna |
Tachyglossus aculeatus (organism) |
| Australian pine pollen allergen |
Australian pine pollen |
| Australian thick-knee |
Burhinus grallarius (organism) |
| Australian thick-knee |
Burhinus giganteus (organism) |
| Autoaugmentation of bladder |
Autoaugmentation of urinary bladder |
| Autoaugmentation of bladder |
Clam cystoplasty |
| transplantation af autogen hudgraft |
Split thickness graft of skin to skin (procedure) |
| transplantation af autogen hudgraft |
Full thickness autograft of skin (substance) |
| autogen vaccine/autogen bakterin |
Vaccine product |
| Autoimmune haemolytic anaemia |
Hemolytic disease of fetus OR newborn due to isoimmunization (disorder) |
| Autoimmune haemolytic anaemia |
Autoimmune hemolytic anemia (disorder) |
| Autoimmune hemolytic anemia |
Hemolytic disease of fetus OR newborn due to isoimmunization (disorder) |
| Autoimmune hemolytic anemia |
Autoimmune hemolytic anemia (disorder) |
| autoimmun progesteron dermatit/urticaria |
Autoimmune progesterone dermatitis |
| autoimmun progesteron dermatit/urticaria |
Menstrual urticaria |
| autologe kondrocytceller 12 millioner, injektionsvæske, opløsning mhp. implantation |
Product containing precisely autologous cultured chondrocyte 30 million unit/1 milliliter conventional release intraarticular implant (clinical drug) |
| Automatic cranial perforator, reusable |
Automatic-releasing cranial perforator |
| Automatic cranial perforator, single-use |
Automatic-releasing cranial perforator |
| Automatic pneumatic pulmonary resuscitator, reusable |
Automatic pulmonary resuscitator (physical object) |
| Automatic pneumatic pulmonary resuscitator, single-use |
Automatic pulmonary resuscitator (physical object) |
| Autonomic nervous system poisoning NOS |
Poisoning by drug AND/OR medicinal substance |
| Autopen 1.5mL one unit device |
Injection device |
| Autopen 1.5mL two unit device |
Injection device |
| Autopen 3mL two unit device |
Injection device |
| Autopen device |
Injection device |
| Autopsied body |
Autopsied body (finding) |
| autosomalt dominant analbuminæmi |
Congenital analbuminemia (CAA) is characterized by the absence or dramatic reduction of circulating human serum albumin (HSA). |
| Autosomal dominant epidermolysis bullosa simplex |
Autosomal dominant epidermolysis bullosa simplex (disorder) |
| Autosomal dominant epidermolysis bullosa simplex |
Epidermolysis bullosa simplex, Ogna type (disorder) |
| Autosomal dominant familial isolated hypoparathyroidism |
Autosomal dominant hypocalcemia (disorder) |
| Autosomal dominant familial isolated hypoparathyroidism |
Hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland (disorder) |
| Autosomal dominant familial isolated hypoparathyroidism |
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) |
| Autosomal dominant familial isolated hypoparathyroidism |
A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism causing hypocalcemia due to insufficient serum levels of bioactive parathormone (PTH), without other endocrine disorders or developmental defects. |
| Autosomal dominant isolated somatotropin deficiency |
Autosomal dominant isolated somatotropin deficiency |
| Autosomal dominant isolated somatotropin deficiency |
Ateliotic dwarfism without insulinopenia (disorder) |
| Autosomal recessive familial isolated hypoparathyroidism |
A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism causing hypocalcemia due to insufficient serum levels of bioactive parathormone (PTH), without other endocrine disorders or developmental defects. |
| Autosomal recessive familial isolated hypoparathyroidism |
Hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland (disorder) |
| Autosomal recessive familial isolated hypoparathyroidism |
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) |
| Autosomal recessiv muskeldystrofi forårsaget af gen med locus på kromosom 15q |
A subtype of autosomal recessive limb girdle muscular dystrophy characterized by a variable age of onset of progressive, typically symmetrical and selective weakness and atrophy of proximal shoulder- and pelvic-girdle muscles (gluteus maximus, thigh adductors, and muscles of the posterior compartment of the limbs are most commonly affected) without cardiac or facial involvement. Clinical manifestations include exercise intolerance, a waddling gait, scapular winging and calf pseudo-hypertrophy. |
| Hereditary sensory and autonomic neuropathy, type II |
Hereditary insensitivity to pain with anhidrosis |
| Hereditary sensory and autonomic neuropathy, type II |
Hereditary sensory and autonomic neuropathy type II (disorder) |
| Hereditary sensory and autonomic neuropathy, type II |
Charcot-Marie-Tooth disease, type II (disorder) |
| Autosomal recessiv spondyloepimetafyseal dysplasi |
Spondyloepimetaphyseal dysplasia, Irapa type is characterized by disproportionate short-trunked short stature, pectus carinatum, short arms, short and broad hands, short metatarsals, flat and broad feet, coxa vara, genu valgum, osteoarthritis, arthrosis and moderate-to-serious gait impairment. |
| Avascular necrosis of femoral condyle (& [medial]) |
Avascular necrosis of medial femoral condyle (disorder) |
| Avian adeno-associated virus |
Muscovy duck parvovirus (organism) |
| Avian adeno-associated virus |
Goose parvovirus (organism) |
| Avian adenovirus 2 antibody |
Turkey adenovirus 3 antibody |
| Avian adenovirus 2 antibody assay |
Measurement of Turkey adenovirus 3 antibody (procedure) |
| Avian herpesvirus |
Gallid herpesvirus 1 (organism) |
| Avian herpesvirus |
Gallid herpesvirus 3 (organism) |
| Avian herpesvirus |
Gallid herpesvirus 2 (organism) |
| Avian herpesvirus |
Anatid herpesvirus 1 (organism) |
| Avian infectious bronchitis virus Ark-99 |
Antibody to Avian infectious bronchitis virus Ark-99 (substance) |
| Avian influenza |
Influenza caused by Influenza A virus (disorder) |
| aviært influenzavirus med høj patogenicitet |
Influenza A virus (organism) |
| aviært influenzavirus med lav patogenicitet |
Influenza A virus (organism) |
| Avian parvovirus |
Goose parvovirus (organism) |
| Avian parvovirus |
Chicken parvovirus (organism) |
| Avian parvovirus |
Muscovy duck parvovirus (organism) |
| Avian reticuloendotheliosis virus |
Reticuloendotheliosis virus (strain T,A) (organism) |
| Avian reticuloendotheliosis virus |
Reticuloendotheliosis virus (organism) |
| Avian sarcoma virus |
Avian sarcoma virus (organism) |
| Avian sarcoma virus |
Rous sarcoma virus (organism) |
| Avian type C oncovirus group |
Genus Alpharetrovirus (organism) |
| Avian type C oncovirus group |
Reticuloendotheliosis virus (organism) |
| Avibactam and ceftazidime |
Product containing avibactam and ceftazidime (medicinal product) |
| Avioserpens species |
Avioserpens (organism) |
| Avocet |
Genus Recurvirostra (organism) |
| Avulsion leg varicose vein (& Babcock) |
Avulsion of varicose vein of leg |
| Avulsion of eye |
Traumatic enucleation of eye |
| Axenfeld's anomaly |
Posterior embryotoxon (disorder) |
| Axenfeld's anomaly |
Axenfeld anomaly |
| Axilla |
Entire axillary fossa |
| Axilla |
Entire axillary fossa |
| Axilla |
Structure of axillary fossa (body structure) |
| Axilla |
Axillary region structure |
| Axilla |
Structure of axillary fossa (body structure) |
| Axilla |
Entire axillary region |
| Axilla |
Axillary region structure |
| Axilla |
Entire axillary region |
| Aksilstruktur |
Axillary region structure |
| Aksilstruktur |
Structure of axillary fossa (body structure) |
| Arteria axillaris og dens grene |
Entire axillary artery |
| Arteria axillaris og dens grene |
Structure of axillary artery |
| aksillær linje i truncus |
Anterior axillary line structure |
| aksillær linje i truncus |
Posterior axillary line structure |
| Axillary vein and its tributaries |
Structure of axillary vein |
| Axillary vein and its tributaries |
Entire axillary vein |
| Axillary-femoral arterial bypass |
Axillary-femoral arterial bypass (procedure) |
| Axillary-femoral arterial bypass |
Superficial axillofemoral vascular bypass (procedure) |
| Axitinib 1mg tablet |
Product containing precisely axitinib 1 milligram/1 each conventional release oral tablet (clinical drug) |
FHIR