| Members |
targetComponentId |
| Mislykket tangforløsning |
Forceps delivery failed (situation) |
| mislykket instrumentel forløsning |
Failed instrumental delivery |
| mislykket igangsættelse af fødsel ved hindesprængning med prænatalt problem |
Failed mechanical induction |
| forsøg på abort uden komplikation |
Failed attempted medical abortion (disorder) |
| Mislykket forløsning vha. vakuumekstraktor |
Failed ventouse delivery (situation) |
| Failure in dose NOS |
Failure in dosage |
| Failure in dose NOS |
Failure in dosage |
| Manglende laktation med prænatal komplikation |
Failure of lactation |
| Manglende laktation med postnatal komplikation |
Failure of lactation |
| Failure of resorption of root of tooth |
Persistent primary tooth (disorder) |
| Failure of sterile precautions during procedure NOS |
Failure of sterile precautions during procedure |
| Failure of sterile precautions during procedure NOS |
Failure of sterile precautions during procedure |
| Falcivibrio |
Mobiluncus |
| Falcivibrio grandis |
Mobiluncus mulieris |
| Falcivibrio species |
Mobiluncus |
| Falcivibrio vaginalis |
Mobiluncus curtisii |
| Fall from or out of building or other structure |
Fall from building |
| Fall from or out of building or other structure |
Fall from building |
| Fall from or out of building or other structure NOS |
Fall from building |
| Fall into hole or other opening in surface |
Fall into hole |
| Fall into hole or other opening in surface |
Fall into hole |
| Fall into other hole or other opening in surface |
Fall into hole |
| Insufflering i tuba uterina, ikke nærmere specificeret |
Inflation of fallopian tube |
| Fallopian insufflation NOS |
Inflation of fallopian tube |
| fund vedr. tuba uterina udtrykt ved TNM-systemet |
American Joint Committee on Cancer allowable value |
| Familial alobar holoprosencephaly |
Holoprosencephaly sequence |
| Familiær amyloid neuropati, finsk type |
A rare systemic amyloidosis with characteristics of a triad of ophthalmologic, neurologic and dermatologic findings due to the deposition of gelsolin amyloid fibrils in these tissues. Clinical manifestations include corneal lattice dystrophy, cranial neuropathy, especially affecting the facial nerve, bulbar signs, cutis laxa, increased skin fragility and less commonly peripheral neuropathy and renal failure. Caused by mutation in the gelsolin gene (GSN). |
| Familiær glomustumor i huden |
Familial benign glomus tumour of skin |
| Familial lambdoid synostosis |
Nonsyndromic premature fusion of a single suture. |
| Familiær lobulær glomerulopati |
A primary glomerular disease with characteristics of proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life. Fibronectin glomerulopathy may present at different ages, although mostly in adolescence or early adulthood, with typical features of a nephrotic syndrome including hypertension. Clustering of the disease within families indicates a genetic origin. In 40% of families, the disease is caused by heterozygous mutations in the FN1 gene (2q34) encoding fibronectin. Whole-genome linkage analysis in a large pedigree showed another disease locus on 1q32, however no specific candidate genes has been identified so far. Segregation with disease appearance in successive generations is consistent with an autosomal dominant pattern of inheritance with age-related penetrance. |
| Café au lait-pletter uden neurofibromatose |
Neurofibromatosis type 6 (NF6), also referred as café-au-lait spots syndrome, is a cutaneous disorder characterized by the presence of several café-au-lait (CAL) macules without any other manifestations of neurofibromatosis or any other systemic disorder. |
| Familial multiple fibrofolliculoma |
Multiple fibrofolliculomas |
| familiære neonatale anfald |
A familial type of self-limited focal epilepsy with onset typically between day two and seven of life. Seizures are focal tonic at onset, affecting the head, face, and limbs. Focal clonic or tonic seizures may evolve to bilateral tonic or clonic seizures. Onset may alternate between hemispheres. Autonomic features (apnea and cyanosis) can be seen. Seizure semiology may progress in a sequential pattern with tonic, clonic, myoclonic and autonomic features following each other without a single predominant feature. Clusters of seizures can occur over hours or days with the neonate behaving normally between events. Developmental progress is usually normal. The electroencephalogram (EEG) background is normal or has minor nonspecific abnormalities. Focal interictal epileptiform abnormalities can be seen in the central, centrotemporal or frontotemporal regions. MRI is normal or has nonspecific findings. Pathogenic variants are seen in KCNQ2, KCNQ3 and SCN2A. |
| Familiar environment |
Familiar environment (finding) |
| Families muridae AND/OR gliridae |
Family Muridae (organism) |
| familien Aceraceae |
Soapberries |
| Family Aceraceae poisoning |
Sapindaceae poisoning (disorder) |
| Acidaminococcaceae |
Family Veillonellaceae (organism) |
| familien Archiangiaceae |
Family Archangiaceae (organism) |
| Family Aspersentidae |
Family Heteracanthocephalidae (organism) |
| Familien Azotobacteraceae |
Subfamily Azobacter group (organism) |
| Family Beggiatoaceae |
Family Thiotrichaceae (organism) |
| Family Catamblyrhynchidae |
Family Thraupidae (organism) |
| Family Caulobacteriaceae |
Family Caulobacteraceae (organism) |
| Family Chamaeidae |
Family Sylviidae (organism) |
| Family Dendrocolaptidae |
Family Furnariidae (organism) |
| Family Dendrocygnidae |
Subfamily Dendrocygninae (organism) |
| familien Fimbriariidae |
Family Fimbriidae |
| familien Hippocastanaceae |
Soapberries |
| Family Myoobiidae |
Family Myobiidae (organism) |
| Family Phytotomidae |
Subfamily Phytotominae (organism) |
| Family Planococaceae |
Family Planococcaceae (organism) |
| Family Pseudoacanthocephalidae |
Family Echinorhynchidae (organism) |
| Familien Rhiziobiaceae |
Family Rhizobiaceae (organism) |
| Family Streblidae - bat fly |
Subfamily Streblinae (organism) |
| familien Thysanosomidae |
Subfamily Thysanosomatinae |
| Family Veillonaceae |
Family Veillonellaceae (organism) |
| Family Zapodidae |
Family Dipodidae (organism) |
| Family apoidea - bee |
Bee |
| Family atelopodidae |
Family Bufonidae |
| Family balaenicipitidae |
Family Pelecanidae (organism) |
| Family cacatuidae |
Family Psittacidae (organism) |
| Family capitonidae |
Subfamily Capitoninae (organism) |
| Family cathartidae |
Family Ciconiidae (organism) |
| Family chironomidae - midge |
Midge |
| Family circumstance NOS |
Details of family - finding |
| Family circumstance NOS |
Details of family - finding |
| Family circumstance NOS |
Details of family - finding |
| Family cochleariidae |
Family Ardeidae (organism) |
| Family cricetidae AND/OR other rat |
Genus Rattus (organism) |
| Family crotalidae - crotalid |
Subfamily Crotalinae (organism) |
| Family cyclarhidae |
Family Vireonidae (organism) |
| Family diomedeidae |
Family Procellariidae (organism) |
| Familieopløsning, ikke nærmere specificeret |
Family disruption |
| Family disruption NOS |
Family disruption |
| Family drepanididae |
Subfamily Drepanidinae (organism) |
| Family dromadidae |
Family Glareolidae (organism) |
| Family haematopodidae |
Family Charadriidae (organism) |
| Family hippocastanaceae poisoning |
Sapindaceae poisoning (disorder) |
| Family history of diabetes mellitus with complication |
Family history of diabetes mellitus (situation) |
| familieanamnese: malignt neoplasme i mamma hos mand |
Family history of malignant neoplasm of breast (situation) |
| slægtning - mentalt handikap |
Family history of intellectual disability |
| familieanamnese: mental retardering |
Family history of intellectual disability |
| slægtning - fysisk handicap |
Family history of disability |
| familieanamnese: alder ved død |
Age of family member at death (observable entity) |
| Family history: Blood disorder NOS |
FH: Blood disorder |
| Family history: Brother NOS |
FH: Brother |
| familieanamnese: kardiovaskulær sygdom, ikke nærmere specificeret |
FH: Cardiovascular disease |
| Family history: Congenital anomaly NOS |
Family history of congenital disease (situation) |
| Family history: Daughter NOS |
Family history with explicit context pertaining to daughter (situation) |
| familieanamnese: lægemiddelafhængighed |
Family history of substance dependency |
| Family history: Ear disorder NOS |
FH: Ear disorder |
| Family history: Endocrine disorder NOS |
Family history of endocrine disorders (situation) |
| Family history: Eye disorder NOS |
FH: Eye disorder |
| Family history: Father NOS |
Family history with explicit context pertaining to father (situation) |
| Family history: Gastrointestinal disorder NOS |
FH: Gastrointestinal disease |
| Family history: Infectious disease NOS |
Family history of infectious disease (situation) |
| familieanamnese: psykisk lidelse, ikke nærmere specificeret |
Family history of mental disorder (situation) |
| familieanamnese: mental retardering |
Family history of intellectual disability |
| Family history: Metabolic disorder NOS |
Family history of metabolic disorder |
| Family history: Mother NOS |
Family history with explicit context pertaining to mother (situation) |
FHIR