| Members |
targetComponentId |
| Congenital bowing: [tibia] &/or [fibula] &/or [femur] |
Congenital bowing of femur |
| Congenital bowing: [tibia] &/or [fibula] &/or [femur] |
Congenital bowing of tibia, fibula and femur |
| Congenital bowing: [tibia] &/or [fibula] &/or [femur] |
Congenital bowing of tibia, fibula and femur |
| Kongenit kapillær proliferation |
Capillary hemangioma |
| Congenital capsular and/or subcapsular cataract |
Congenital capsular cataract |
| Congenital capsular and/or subcapsular cataract |
Congenital subcapsular cataract |
| kongenit malrotation af hjertet |
Congenital malrotation of heart |
| kongenit malrotation af hjertet |
Congenital levorotation of heart (disorder) |
| Congenital cataract |
Congenital cataract |
| Congenital cataract and lens anomalies (& [lens anomaly]) |
Congenital anomaly of lens |
| Kongenitte katarakt- eller linseanomalier |
Congenital anomaly of lens |
| Kongenitte katarakt- eller linseanomalier |
Congenital cataract |
| Kongenit cøliaki |
Celiac disease (disorder) |
| Congenital cerebellar cortical atrophy |
Congenital cerebellar cortical atrophy (disorder) |
| Congenital cerebral arteriovenous: [aneurysm] or [fistula] or [malformation] |
Congenital arteriovenous fistula of brain |
| Congenital cerebral arteriovenous: [aneurysm] or [fistula] or [malformation] |
Cerebral arteriovenous malformation |
| Congenital cerebral arteriovenous: [aneurysm] or [fistula] or [malformation] |
Congenital cerebral arteriovenous aneurysm |
| Congenital cerebral palsy (& spastic) |
A form of spastic cerebral palsy affecting two limbs; usually the legs are affected more than the arms. |
| Congenital cerebral palsy (& spastic) |
A type of cerebral palsy defined by increased tone and pathological reflexes resulting in an abnormal pattern of movement and posture. |
| Kongenit hjernelammelse |
A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain. |
| Kongenit deformitet af thoraxvæggen, ikke klassificeret andetsteds |
Congenital deformity of chest wall |
| Congenital chest wall deformity NEC |
Congenital deformity of chest wall |
| Congenital choledochal cyst |
Congenital choledochal cyst (disorder) |
| Congenital choledochal cyst |
Choledochocele (disorder) |
| Congenital cleft hand |
Congenital cleft hand |
| Congenital cleft hand |
Ectrodactyly |
| kongenit klikkende hofteled |
Neonatal clicking hip |
| Congenital clicking hip |
Neonatal clicking hip |
| Congenital club: [hand] or [fingers] |
Talipomanus |
| Congenital constriction ring with lymphoedema |
Constriction ring of upper limb with lymphedema |
| Congenital cranial osteoporosis |
Craniotabes |
| Congenital cyst of canal of Nuck |
Hydrocele of canal of Nuck |
| Congenital cyst of canal of Nuck |
Congenital cyst of canal of Nuck |
| Kongenit cystisk øre |
Preauricular cyst |
| kongenitte cyster i det posteriore segment |
Congenital cyst of posterior segment of eye |
| kongenit debilitet hos foster |
Neonatal disorder |
| kongenit debilitet hos foster |
Failure to thrive |
| kongenit debilitet hos foster |
Fetal disorder |
| Congenital deformities: [skull] &/or [face] &/or [jaw] |
Congenital anomaly of jaw |
| Congenital deformity of clavicle (& [agenesis]) |
Congenital deformity of clavicle |
| Congenital deformity of clavicle (& [agenesis]) |
Agenesis of clavicle |
| Congenital diaphragmatic: [hernia] or [defect NEC] |
Congenital diaphragmatic hernia |
| Congenital diplegia |
A form of spastic cerebral palsy affecting two limbs; usually the legs are affected more than the arms. |
| Congenital diplegia |
A form of spastic cerebral palsy affecting the lower half of the body, including both legs. |
| kongenit sygdom og abnormitet af hjertet, pars thoracica aortae og perikardiet |
Multiple system malformation syndrome |
| Kongenit luksation og subluksation i hofte |
Congenital dislocation of hip |
| Congenital dislocation of elbow |
Dislocation of joint of upper limb |
| Congenital dislocation of elbow |
Congenital dislocation of elbow (disorder) |
| Kongenit luksation af én hofte med subluksation af den anden |
Congenital dislocation of left hip co-occurrent with congenital subluxation of right hip (disorder) |
| Kongenit luksation af én hofte med subluksation af den anden |
Congenital dislocation of right hip co-occurrent with congenital subluxation of left hip (disorder) |
| kongenitte forstyrrelser af øjen- og øjenlågsbevægelser |
Movement of eyelid - finding |
| kongenitte forstyrrelser af øjen- og øjenlågsbevægelser |
Congenital structural abnormality of eyelid |
| kongenitte forstyrrelser af øjen- og øjenlågsbevægelser |
Congenital anomaly of eye |
| Congenital displaced uterus (& [prolapse]) |
Malposition of uterus |
| Congenital displaced uterus (& [prolapse]) |
Congenital prolapsed uterus |
| Congenital diverticulum of esophagus |
Congenital diverticulum of esophagus |
| Congenital dystrophia brevicollis |
Congenital dystrophia brevicollis (disorder) |
| Congenital dystrophia brevicollis |
Turner syndrome |
| Kongenit ektodermal dysplasi af ansigtet |
Focal facial dermal dysplasias (FFDD) are rare ectodermal dysplasias, with characteristics of congenital bitemporal (resembling forceps marks) or preauricular scar-like lesions associated with additional facial and or systematic manifestations. Four types of FFDD are described. Types II and III present with a variable facial dysmorphism including distichiasis (upper lashes) or lacking eyelashes, and upward slanting and thinned lateral eyebrows with a flattened nasal bridge and full upper lip. Types I and IV are infrequently associated with extra-cutaneous anomalies. |
| Congenital ectopia (morphologic abnormality) |
Choristoma (morphologic abnormality) |
| Congenital ectopia (morphologic abnormality) |
Congenital ectopia (morphologic abnormality) |
| Congenital epulis of newborn |
Congenital epulis of newborn |
| Congenital epulis of newborn |
Congenital gingival granular cell tumor |
| Congenital exostosis (& [multiple]) |
Congenital exostosis |
| Congenital exostosis (& [multiple]) |
Multiple congenital exostosis |
| kongenit ansigts- eller halsanomali, ikke nærmere specificeret |
Congenital anomaly of face (disorder) |
| kongenit ansigts- eller halsanomali, ikke nærmere specificeret |
Congenital anomaly of neck |
| kongenit sammenvoksningsdefekt med hernie |
Developmental failure of fusion (morphologic abnormality) |
| Kongenit facial dystrofi |
Stiff skin syndrome is a rare, slowly progressive cutaneous disease characterized by rock-hard skin bound firmly to the underlying tissues (mainly on the shoulders, lower back, buttocks and thighs), mild hypertrichosis and hyperpigmentation overlying the affected areas of skin, as well as limited joint mobility (mainly of large joints) with flexion contractures. Cutaneous nodules, affecting mostly distal interphalangeal joints, as well as extracutaneous manifestations, including diffuse entrapment neuropathy, scoliosis, a tiptoe gait and a narrow thorax, may be associated. Restrictive pulmonary changes, muscle weakness, short stature and growth delay have also been reported. No vascular hyperreactivity, immunologic abnormalities nor visceral, muscular or bone involvement has been described. |
| Congenital fusion of spine (& [lumbosacral]) |
Congenital lumbosacral fusion |
| Congenital fusion of spine (& [lumbosacral]) |
Congenital fusion of spine |
| Congenital glaucoma |
Buphthalmos (finding) |
| Congenital glaucoma |
Buphthalmos (finding) |
| Congenital glaucoma |
Primary congenital glaucoma (disorder) |
| Congenital glaucoma |
Primary congenital glaucoma (disorder) |
| Congenital hallux valgus |
Congenital hallux valgus |
| Congenital hallux valgus |
Hallux valgus (disorder) |
| Congenital heart and cardiac apex malposition (& [ectopic heart]) |
Ectopia cordis |
| Congenital heart and cardiac apex malposition (& [ectopic heart]) |
Congenital malposition of heart |
| kongenit hjerteanomali, ikke nærmere specificeret |
Congenital heart disease |
| Congenital heart anomaly NOS |
Congenital heart disease |
| Kongenit hyperammonæmi, type I |
A rare, severe disorder of urea cycle metabolism typically characterized by either a neonatal onset of severe hyperammonemia that occurs few days after birth and manifests with lethargy, vomiting, hypothermia, seizures, coma and death or a presentation outside the newborn period at any age with (sometimes) milder symptoms of hyperammonemia. |
| kongenit hyperrotation |
Congenital malrotation |
| Congenital hypertrophy of eye bulge |
Congenital hypertrophy of retinal pigment epithelium |
| Congenital hypertrophy of eye bulge |
Congenital exophthalmos |
| Kongenit hypodonti, multiple tænder, i relation til systemisk sygdom |
Anodontia |
| Kongenit hypodonti, multiple tænder, i relation til systemisk sygdom |
Partial congenital absence of teeth |
| Kongenit hypodonti, multiple tænder, uden relation til systemisk sygdom |
Partial congenital absence of teeth |
| Kongenit hypodonti, multiple tænder, uden relation til systemisk sygdom |
Anodontia |
| Congenital hypoplasia of renal papilla |
Congenital small renal papilla |
| Congenital hypoplasia of renal papilla |
Congenital hypoplasia of renal papilla |
| Congenital hypothyroidism: [cretinism] or [NOS] |
Congenital hypothyroidism |
| Congenital hypotonia |
Neonatal hypotonia |
| Congenital hypotonia |
Floppy infant syndrome |
| Congenital infection: [NOS] or [cytomegalovirus] or [herpes simplex] or [toxoplasmosis] |
Congenital toxoplasmosis |
| Congenital infection: [NOS] or [cytomegalovirus] or [herpes simplex] or [toxoplasmosis] |
Congenital cytomegalovirus infection |
| Congenital infection: [NOS] or [cytomegalovirus] or [herpes simplex] or [toxoplasmosis] |
Congenital toxoplasmosis |
| Congenital infection: [NOS] or [cytomegalovirus] or [herpes simplex] or [toxoplasmosis] |
Congenital cytomegalovirus infection |
| Congenital integument anomalies (& [birthmark NOS]) |
Congenital anomaly of integument |
| Congenital kyphoscoliosis |
Acquired kyphoscoliosis (disorder) |
| Congenital kyphoscoliosis |
Congenital kyphoscoliosis (disorder) |
FHIR