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900000000000526001: REPLACED BY association reference set (foundation metadata concept)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT model component module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module
900000000001156010 REPLACED BY association reference set (foundation metadata concept) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)
900000000001157018 REPLACED BY association reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)


23753 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
REPLACED BY association reference set (foundation metadata concept) Is a Historical association reference set (foundation metadata concept) true Inferred relationship Some

Members targetComponentId
Cone biopsy of cervix uteri NEC Cone biopsy of cervix
Cone biopsy of cervix uteri NEC Cone biopsy of cervix
Cone cells of inner nuclear layer Cone of retina
Cone monochromatism Blue cone monochromatism (disorder)
Confidential data NOS Confidential patient data held
Confidential data NOS Confidential patient data held
Confirming patient identity by direct questioning Verification of identity by direct questioning (procedure)
Confirming patient identity by guardian interview Verification of identity using information from guardian (procedure)
Confirming patient identity by wristband Verification of identity using information on identification band (procedure)
Confirming patient identity prior to procedure Verification of identity prior to procedure (procedure)
Congener toxicity Polychlorinated biphenyl poisoning
Congenital CNS anomalies NOS Congenital anomaly of central nervous system
Congenital CNS anomalies NOS Congenital anomaly of central nervous system
Congenital CNS anomalies NOS Congenital anomaly of central nervous system
Congenital CVS anomaly NOS Congenital anomaly of cardiovascular system
Congenital CVS anomaly NOS Congenital anomaly of cardiovascular system
Congenital CVS anomaly NOS Congenital anomaly of cardiovascular system
Congenital abnormal fusion Abnormally fused structure (morphologic abnormality)
Congenital abnormal number Abnormal number (morphologic abnormality)
Congenital abnormality of uterus affecting obstetric care Congenital abnormality of uterus in pregnancy, childbirth and the puerperium
Congenital anomaly NOS Congenital malformation
Congenital anomaly NOS Congenital malformation
Congenital anomaly NOS Congenital malformation
Congenital anomaly NOS Congenital malformation
Congenital anomaly: [upper GIT NOS] or [oesophagus] Congenital malformation of upper alimentary tract
Congenital anomaly: [upper GIT NOS] or [oesophagus] Congenital malformation of upper alimentary tract
Congenital atresia Atresia (morphologic abnormality)
Congenital atresia of pulmonary valve NOS Congenital atresia of pulmonary valve
Congenital cataract Opacity
Congenital cerebral cyst NOS Congenital cyst of brain (disorder)
Congenital cerebral palsy NOS Cerebral palsy
Congenital cerebral palsy NOS Cerebral palsy
Congenital cystic dilatation with accumulation of fluid Cystic dilatation with accumulation of fluid
Congenital deformity Deformity
Congenital dislocation of hip NOS Congenital dislocation of hip
Congenital dislocation of hip NOS Congenital dislocation of hip
Congenital dystrophia brevicollis Klippel-Feil sequence
Congenital dystrophia brevicollis Klippel-Feil sequence
Congenital endaural hernia Encephalocele
Congenital giant pigmented nevus of skin Large congenital pigmented melanocytic nevus of skin (disorder)
Congenital hereditary endothelial dystrophy type 1 Polymorphous corneal dystrophy
Congenital imperforation, high Atresia (morphologic abnormality)
Congenital imperforation, low Atresia (morphologic abnormality)
Congenital incomplete expansion of lung Perinatal atelectasis
Congenital leukocyte adherence deficiency Leukocyte adhesion deficiency
Congenital lordosis Congenital lordosis deformity of spine (disorder)
Congenital macrocolon, not aganglionic Congenital dilatation of colon
Congenital malformation syndromes affecting facial appearance Multiple malformation syndrome with facial defects as major feature
Congenital malformation syndromes involving limbs Multiple malformation syndrome with limb defect as major feature
Congenital malposition, left Left malposition (morphologic abnormality)
Congenital malposition, right Right malposition (morphologic abnormality)
Congenital medial deviation Medial displacement
Congenital melanocytic nevus Pigmented nevus
Congenital misalignment Misalignment (morphologic abnormality)
Congenital musculoskeletal anomalies NOS Congenital anomaly of musculoskeletal system
Congenital musculoskeletal anomalies NOS Congenital anomaly of musculoskeletal system
Congenital myelin deficiency of the optic disc Congenital anomaly of optic disc
Congenital night blindness NOS Congenital stationary night blindness
Congenital pancreatic enterokinase deficiency Intestinal enteropeptidase deficiency
Congenital postural lordosis Congenital lordosis deformity of spine (disorder)
Congenital premature fusion Premature fusion
Congenital pseudoarthrosis Pseudoarthrosis
Congenital ridge ear Congenital deformity of pinna
Congenital sequestration Sequestration (morphologic abnormality)
Congenital smallness Abnormal smallness (morphologic abnormality)
Congenital thrombocytopenic purpura Upshaw-Schulman syndrome (disorder)
Congenital trigger thumb Pediatric trigger thumb
Congenital trigger thumb of bilateral hands Pediatric locking of interphalangeal joint of bilateral thumbs (disorder)
Congenital trigger thumb of left hand Pediatric trigger thumb of left hand
Congenital trigger thumb of right hand Pediatric locking of interphalangeal joint of right thumb (disorder)
Congenital von Willebrand's disease Hereditary von Willebrand disease
Congenital von Willebrand's disease type I Hereditary von Willebrand disease type 1
Congenital von Willebrand's disease type II Hereditary von Willebrand disease type 2
Congestive heart failure clinical management plan Congestive heart failure clinical management plan (record artifact)
Congo hemorrhagic fever Congo-Crimean hemorrhagic fever (disorder)
Conjoined twins causing disproportion Disproportion between fetus and pelvis due to conjoined twins (disorder)
Conjoined twins causing disproportion Disproportion between fetus and pelvis due to conjoined twins (disorder)
Conjunctival swab taken Taking conjunctival swab
Conjunctival swab taken for virology Taking conjunctival swab
Connection between lacrimal gland and nose NOS Creation of anastomosis between lacrimal drainage system and nose (procedure)
Connection of organ NOC Surgical procedure (procedure)
Connection of organ NOC NOS Surgical procedure (procedure)
Connection of organ NOC OS Surgical procedure (procedure)
Connection of stomach to duodenum NEC Anastomosis of stomach
Connection of stomach to duodenum NOS Anastomosis of stomach
Connective tissue by site Connective tissue structure
Connective tissue disorder by body site Disorder of connective tissue (disorder)
Connective tissue gingival graft Grafting of connective tissue to gingiva (procedure)
Consciousness disturbance NOS Disturbance of consciousness
Consciousness disturbance NOS Disturbance of consciousness
Constipation NOS Constipation
Constipation NOS Constipation
Constipation NOS Constipation
Construction manager NOS Construction manager
Construction manager NOS Construction manager
Construction worker NOS Construction worker
Construction worker NOS Construction worker
Construction/mining NOS Construction/mining workers
Construction/mining NOS Construction/mining workers
Contact dermatitis NOS Contact dermatitis
Contact dermatitis NOS Contact dermatitis

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