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900000000000523009: POSSIBLY EQUIVALENT TO 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
900000000001150016 POSSIBLY EQUIVALENT TO 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)
900000000001151017 POSSIBLY EQUIVALENT TO association reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)


49567 members. Search Members:

Expanded Value Set


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

Members targetComponentId
Kongenit subtotal katarakt Congenital zonular cataract
Congenital syphilis: [early forms - named variants] Congenital syphilitic chronic coryza
Congenital syphilis: [early forms - named variants] Early congenital syphilis with symptoms
Congenital talipes calcaneus Congenital talipes calcaneus
Congenital trigger finger and trigger thumb Pediatric trigger thumb
Congenital trigger finger and trigger thumb Congenital trigger finger
kongenit vendende nedad Malposition (morphologic abnormality)
kongenit vendende nedad Deformity (morphologic abnormality)
Medfødt opaddrejning Malposition (morphologic abnormality)
Medfødt opaddrejning Deformity (morphologic abnormality)
Congenital undergrowth of distal part of limb (& lower limb) Congenital anomaly of limb
Congenital undergrowth of distal part of limb (& lower limb) Congenital anomaly of lower limb
Congenital undergrowth of proximal part of limb Congenital anomaly of lower limb
Congenital undergrowth of proximal part of limb Congenital anomaly of limb
Kongenit manglende hemidiaphragma – unilateralt Congenital absence of right hemidiaphragm (disorder)
Kongenit manglende hemidiaphragma – unilateralt Congenital absence of left hemidiaphragm (disorder)
unilateral kongenit hofteluksation Congenital subluxation of right hip joint
unilateral kongenit hofteluksation Congenital subluxation of left hip joint
unilateral kongenit vesikoureterorenal refluks Congenital left vesicoureterorenal reflux
unilateral kongenit vesikoureterorenal refluks Congenital right vesicoureterorenal reflux
Congenital urethral: [valvular stricture] or [posterior valves] or [posterior valvular stricture] Congenital urethral posterior valvular stricture
Congenital urethral: [valvular stricture] or [posterior valves] or [posterior valvular stricture] Congenital urethral valvular stricture
Congenital urethral: [valvular stricture] or [posterior valves] or [posterior valvular stricture] Congenital posterior urethral valves
Congenital urinary anomalies (& [anomaly kidney]) Congenital anomaly of the kidney
Congenital urinary anomalies (& [anomaly kidney]) Congenital anomaly of the kidney
Congenital urinary anomalies (& [anomaly kidney]) Congenital malformation of the urinary system
Congenital urinary anomalies (& [anomaly kidney]) Congenital malformation of the urinary system
Congenital uterine abnormality (& [bicornuate uterus]) Congenital uterine anomaly
Congenital uterine abnormality (& [bicornuate uterus]) Bicornuate uterus
Congenital uterine abnormality (& [bicornuate uterus]) Bicornuate uterus
Congenital uterine anomaly (& [bicornuate uterus]) Congenital uterine anomaly
Congenital uterine anomaly (& [bicornuate uterus]) Bicornuate uterus
Congenital uterine anomaly (& [bicornuate uterus]) Congenital uterine anomaly
Congenital uterine anomaly (& [bicornuate uterus]) Bicornuate uterus
Congenital uterus abnormality (& [bicornuate] or [double]) in pregnancy, childbirth, puerperium Congenital abnormality of uterus in pregnancy, childbirth and the puerperium
Congenital uterus abnormality (& [bicornuate] or [double]) in pregnancy, childbirth, puerperium Bicornuate uterus in pregnancy, childbirth and the puerperium
Congenital uterus abnormality (& [bicornuate]) in pregnancy, childbirth or the puerperium NOS Congenital abnormality of uterus in pregnancy, childbirth and the puerperium
Congenital valgus: [talipes] or [clubfoot] Congenital talipes calcaneovalgus
Congenital valgus: [talipes] or [clubfoot] Talipes valgus
kongenit varicellainfektion Perinatal varicella
kongenit varicellainfektion Congenital varicella syndrome
Congenital vascular disease Congenital vascular malformation (disorder)
Congenital vascular disease Congenital vascular disorder (disorder)
kongenit vaskulær misdannelse af orbita Congenital malformation of blood vessel of orbit proper (disorder)
kongenit vaskulær misdannelse af orbita Congenital vascular malformation of orbital region (disorder)
Komplet kongenit vaskulær misdannelse Vascular malformation (morphologic abnormality)
Partiel kongenit vaskulær misdannelse Vascular malformation (morphologic abnormality)
Kongenit/genetisk syndrom med poikiloderma Hereditary sclerosing poikiloderma (disorder)
Kongenit/hereditær cutis laxa Inherited cutis laxa
Kongenit/hereditær hypermelanotisk sygdom Hereditary hypermelanosis (disorder)
Kongenit/hereditær hypermelanotisk sygdom Genetic syndrome with hypermelanosis (disorder)
Kongenit/hereditær lentiginose Familial generalized lentiginosis is a rare, inherited, skin hyperpigmentation disorder characterized by widespread lentigines without associated noncutaneous abnormalities. Patients present multiple brown to dark brown, non-elevated macula of 0.2 to 1 cm in diameter, spread over the entire body, sometimes including palms or soles, but never oral mucosa.
Kongenit/hereditær lentiginose Lentiginosis (disorder)
Congenital: [ear/face/neck problem] or [anomaly ear] or [anomaly neck] Congenital malformation of ear
Congenital: [ear/face/neck problem] or [anomaly ear] or [anomaly neck] Ear, face and neck congenital anomalies
Congenital: [ear/face/neck problem] or [anomaly ear] or [anomaly neck] Congenital anomaly of neck
Congenital: [ear/face/neck problem] or [anomaly ear] or [anomaly neck] Congenital malformation of ear
Congenital: [neutropenia] or [agranulocytosis NEC] Congenital neutropenia
Congestive cardiomyopathy Primary dilated cardiomyopathy
Congestive cardiomyopathy Congestive cardiomyopathy (disorder)
Congestive cardiomyopathy Congestive cardiomyopathy (disorder)
Congestive cardiomyopathy Primary dilated cardiomyopathy
Coniothyrium-art Coniothyrium
Conisation of cervix Cold knife cone biopsy of cervix (procedure)
Conisation of cervix (& knife) Excision of cervix by cryoconization (procedure)
Conisation of cervix (& knife) Cold knife cone biopsy of cervix (procedure)
Conisation of cervix Cone biopsy of cervix
Conisation of cervix Excision of cervix by cryoconization (procedure)
Conisation of cervix (& knife) Cone biopsy of cervix
Conjugate gaze palsy Supranuclear paralysis
Conjugate gaze palsy Palsy of conjugate gaze
konjugerede østrogener, syntetisk A Conjugated estrogen
konjugerede østrogener, syntetisk B Conjugated estrogen
konjunktival kirtel Structure of conjunctival gland (body structure)
konjunktival kirtel Entire conjunctival gland
konjunktival inklusionscyste Epithelial inclusion cyst of conjunctiva (disorder)
Conjunctival operation Operation on conjunctiva (procedure)
Conjunctival pigmentations Conjunctival argyrosis
Conjunctival sac instillation Applying medication to eyes
Conjunctival sac instillation Topical local anesthetic to eye
Conjunctival sac instillation Instillation of eye drops to eye (procedure)
Conjunctival sac instillation Applying ointment to eye
Conjunctival xerosis (& [xerophthalmia]) Conjunctival xerosis
Conjunctival xerosis (& [xerophthalmia]) Xerophthalmia
Conjunctivitis &/or unspecified acute conjunctivitis Conjunctivitis
Conjunctivitis: [Newcastle] or [other viral] Infection of eye caused by Avian Paramyxovirus 1 (disorder)
Conjunctivitis: [pseudomembranous] or [membranous] Pseudomembranous conjunctivitis
Conjunctivitis: [pseudomembranous] or [membranous] Membranous conjunctivitis
Conjunctivodacryocystorhinostomy Conjunctivorhinostomy with insertion of stent
Conjunctivodacryocystorhinostomy Conjunctivodacryocystostomy (procedure)
Conjunctivodacryocystorhinostomy Conjunctivorhinostomy (procedure)
Conjunctivodacryocystorhinostomy Stallard operation (procedure)
Conjunctivorhinostomy Conjunctivodacryocystostomy (procedure)
Conjunctivorhinostomy Conjunctivorhinostomy with insertion of stent
Conjunctivorhinostomy Conjunctivorhinostomy (procedure)
Conjunctivorhinostomy Stallard operation (procedure)
Cohen-kanyle Cohen cannula
Cohen-kanyle Kahn cannula (physical object)
Tilslutning af mammaarterie til koronararterie, ikke nærmere specificeret Internal mammary-coronary artery bypass graft
Conradi-Hunermann syndrome Chondrodysplasia punctata, Conradi-Hünermann type (disorder)
Conradi-Hunermann syndrome A rare genodermatosis disease with great phenotypic variation and most common characteristic of ichthyosis following the lines of Blaschko, chondrodysplasia punctata (CDP), asymmetric shortening of the limbs, cataracts and short stature. Caused by mutations in the EBP gene (Xp11.23-p11.22) encoding the emopamil binding protein (EBP), which acts as a delta8-delta7-sterol isomerase that catalyzes the conversion of 8(9)-cholestenol to lathosterol in the distal cholesterol biosynthesis pathway. A deficiency in EBP leads to the accumulation of 8-dehydrocholesterol (8DHC) and 8(9)-cholestenol in the skin, plasma and other body tissues.

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