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721000172106: Belgian GP subset (foundation metadata concept)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 15-Mar 2021. Module: Belgian module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module
1523121000172117 Belgian GP subset (foundation metadata concept) en Fully specified name Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
1523151000172111 Belgian GP subset en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
1523141000172114 sous-ensemble belge pour les médecins généralistes fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
1523131000172119 Belgische subset voor huisartsen nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)

12018 members. Search Members:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Belgian GP subset (foundation metadata concept) Is a Simple type reference set (foundation metadata concept) true Inferred relationship Some
Members
Congenital anomaly of cardiac chamber (disorder)
Congenital anomaly of cerebrovascular system
Congenital anomaly of cornea
Congenital anomaly of coronary artery
Congenital anomaly of esophagus
Congenital anomaly of eye
Congenital anomaly of face (disorder)
Congenital anomaly of fixation of intestine
Congenital anomaly of heart valve
Congenital anomaly of large intestine
Congenital anomaly of larynx
Congenital anomaly of lower limb (disorder)
Congenital anomaly of lung
Congenital anomaly of male genital system
Congenital anomaly of metatarsal bone
Congenital anomaly of musculoskeletal system
Congenital anomaly of nervous system
Congenital anomaly of nose
Congenital anomaly of peripheral blood vessel (disorder)
Congenital anomaly of pharynx
Congenital anomaly of pituitary gland
Congenital anomaly of pleural folds
Congenital anomaly of renal pelvis
Congenital anomaly of rib
Congenital anomaly of sacral vertebra
Congenital anomaly of skin
Congenital anomaly of skull
Congenital anomaly of spine
Congenital anomaly of the kidney
Congenital anomaly of the pelvis
Congenital anomaly of the urinary tract proper (disorder)
Congenital anomaly of thoracic cage
Congenital anomaly of trachea
Congenital anteversion of femur
Congenital arterial aneurysm
Congenital arteriovenous malformation
Congenital atresia of esophagus
Congenital atresia of the pulmonary valve (disorder)
Congenital atresia of ureter
Congenital atrial septal defect (disorder)
Congenital biliary atresia
Congenital bladder neck stenosis
Congenital blindness
Congenital capsular cataract
Congenital cataract
Congenital cerebral hernia
Congenital cerebral meningocele
Congenital cyst of canal of Nuck
Congenital cystic disease of liver
Congenital cystic kidney disease
Congenital cytomegalovirus infection
Congenital deafness
Congenital deformity of chest wall
Congenital deformity of foot (disorder)
Congenital deformity of forehead
Congenital deformity of knee joint
Congenital deformity of spine
Congenital deviation of nasal septum
Congenital dilatation of ureter (disorder)
Congenital dislocation of hip
Congenital dislocation of left hip (disorder)
Congenital dislocation of patella
Congenital dislocation of right hip (disorder)
Congenital dislocation of the hip screening
Congenital chromosomal disease
Congenital duplication of biliary duct
Congenital duplication of renal collecting system
Congenital diverticulum of esophagus
Congenital exostosis
Congenital genu recurvatum
Congenital genu valgum
Congenital genu varum
Congenital glaucoma
Congenital hallux valgus
Congenital hammer toe (disorder)
Congenital hearing disorder
Congenital heart disease
Congenital hip dysplasia
Congenital hydrocele
Congenital hydrocephalus
Congenital hydronephrosis
Congenital hypertrophy of cardiac ventricle
Congenital hypertrophy of retinal pigment epithelium
Congenital hypoplasia of breast
Congenital hypoplasia of kidney
Congenital hypothyroidism
Congenital ichthyosis of skin
Congenital infectious disease
Congenital insufficiency of mitral valve (disorder)
Congenital insufficiency of tricuspid valve
Congenital iodine deficiency syndrome
Congenital kyphoscoliosis (disorder)
Congenital lactase deficiency
Congenital laryngeal stridor
Congenital laryngomalacia
Congenital leg bone bowing
Congenital leg length discrepancy (disorder)
Congenital macrocephaly (disorder)
Congenital malformation
Congenital malformation of ear
Congenital malformation of genital organs (disorder)

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