| Members |
acceptabilityId |
| 999 (qualifier value) |
Preferred (foundation metadata concept) |
| 999.34 |
Preferred (foundation metadata concept) |
| 999.34 (qualifier value) |
Preferred (foundation metadata concept) |
| 99m-Rh |
Acceptable (foundation metadata concept) |
| 99m-Tc |
Acceptable (foundation metadata concept) |
| 99mTc-HMPAO |
Acceptable (foundation metadata concept) |
| 9Fr |
Acceptable (foundation metadata concept) |
| 9am cortisol level |
Preferred (foundation metadata concept) |
| 9am cortisol level |
Preferred (foundation metadata concept) |
| 9am cortisol level |
Acceptable (foundation metadata concept) |
| 9am cortisol level (procedure) |
Preferred (foundation metadata concept) |
| 9am cortisol level (procedure) |
Preferred (foundation metadata concept) |
| 9am cortisol measurement |
Preferred (foundation metadata concept) |
| 9am cortisol measurement (procedure) |
Preferred (foundation metadata concept) |
| 9p deletion syndrome |
Acceptable (foundation metadata concept) |
| 9p minus syndrome |
Acceptable (foundation metadata concept) |
| 9p monosomy syndrome |
Acceptable (foundation metadata concept) |
| 9p partial monosomy syndrome |
Preferred (foundation metadata concept) |
| 9p partial monosomy syndrome (disorder) |
Preferred (foundation metadata concept) |
| 9p partial trisomy syndrome |
Preferred (foundation metadata concept) |
| 9p partial trisomy syndrome (disorder) |
Preferred (foundation metadata concept) |
| 9p13 microdeletion syndrome |
Preferred (foundation metadata concept) |
| 9p13 microdeletion syndrome (disorder) |
Preferred (foundation metadata concept) |
| 9p13 microdeletion syndrome is a rare chromosomal anomaly syndrome, resulting from a partial interstitial deletion of the short arm of chromosome 9, characterized by mild to moderate developmental delay, hand tremors, myoclonic jerks, attention deficit-hyperactivity disorder and a social personality. Patients also present bruxism, short stature and minor facial dysmorphic features (e.g., bilateral epicanthic folds, broad, flat nasal bridge, anteverted nares, low-set ears micro/retro-gnathia). |
Preferred (foundation metadata concept) |
| 9p24.3 deletion syndrome |
Preferred (foundation metadata concept) |
| 9p24.3 deletion syndrome (disorder) |
Preferred (foundation metadata concept) |
| 9q partial monosomy syndrome |
Preferred (foundation metadata concept) |
| 9q partial monosomy syndrome (disorder) |
Preferred (foundation metadata concept) |
| 9q partial trisomy syndrome |
Preferred (foundation metadata concept) |
| 9q partial trisomy syndrome (disorder) |
Preferred (foundation metadata concept) |
| 9q21.13 microdeletion syndrome |
Preferred (foundation metadata concept) |
| 9q21.13 microdeletion syndrome (disorder) |
Preferred (foundation metadata concept) |
| 9q22.3 deletion syndrome |
Preferred (foundation metadata concept) |
| 9q22.3 deletion syndrome |
Acceptable (foundation metadata concept) |
| 9q22.3 deletion syndrome (disorder) |
Preferred (foundation metadata concept) |
| 9q31.1q31.3 microdeletion syndrome |
Preferred (foundation metadata concept) |
| 9q31.1q31.3 microdeletion syndrome (disorder) |
Preferred (foundation metadata concept) |
| 9q33.3q34.11 microdeletion syndrome |
Preferred (foundation metadata concept) |
| 9q33.3q34.11 microdeletion syndrome (disorder) |
Preferred (foundation metadata concept) |
| 9q34 deletion syndrome |
Preferred (foundation metadata concept) |
| 9q34 deletion syndrome (disorder) |
Preferred (foundation metadata concept) |
| 9th floor |
Acceptable (foundation metadata concept) |
| 9x/day |
Acceptable (foundation metadata concept) |
| :: Gamma heavy chain disease |
Acceptable (foundation metadata concept) |
| < |
Preferred (foundation metadata concept) |
| < 4 mitoses/high power field |
Preferred (foundation metadata concept) |
| < 4 mitoses/high power field (finding) |
Preferred (foundation metadata concept) |
| <1.5 hours sent off: [DS4] or [DS1500] |
Preferred (foundation metadata concept) |
| <1.5 hours sent off: [DS4] or [DS1500] (finding) |
Preferred (foundation metadata concept) |
| <2 fingers |
Preferred (foundation metadata concept) |
| <2 fingers (qualifier value) |
Preferred (foundation metadata concept) |
| <3 |
Preferred (foundation metadata concept) |
| <3 (qualifier value) |
Preferred (foundation metadata concept) |
| <35 degrees C |
Acceptable (foundation metadata concept) |
| <90 |
Preferred (foundation metadata concept) |
| <90 (qualifier value) |
Preferred (foundation metadata concept) |
| <90 degrees |
Preferred (foundation metadata concept) |
| <90 degrees (qualifier value) |
Preferred (foundation metadata concept) |
| <= |
Preferred (foundation metadata concept) |
| = |
Preferred (foundation metadata concept) |
| > |
Preferred (foundation metadata concept) |
| > 4 mitoses/high power field |
Acceptable (foundation metadata concept) |
| >10 mitoses per 10 HPF (score = 3) |
Acceptable (foundation metadata concept) |
| >2 fingers |
Preferred (foundation metadata concept) |
| >2 fingers (qualifier value) |
Preferred (foundation metadata concept) |
| >2.5 hours sent off: [DS4] or [DS1500] |
Preferred (foundation metadata concept) |
| >2.5 hours sent off: [DS4] or [DS1500] (finding) |
Preferred (foundation metadata concept) |
| >20 mitoses per 10 HPF (score = 3) |
Acceptable (foundation metadata concept) |
| >35 degrees C |
Acceptable (foundation metadata concept) |
| >4 cusps |
Preferred (foundation metadata concept) |
| >4 cusps (qualifier value) |
Preferred (foundation metadata concept) |
| >5 |
Preferred (foundation metadata concept) |
| >5 (qualifier value) |
Preferred (foundation metadata concept) |
| >50 degrees C |
Acceptable (foundation metadata concept) |
| >90 |
Preferred (foundation metadata concept) |
| >90 (qualifier value) |
Preferred (foundation metadata concept) |
| >90 degrees |
Preferred (foundation metadata concept) |
| >90 degrees (qualifier value) |
Preferred (foundation metadata concept) |
| >97 |
Preferred (foundation metadata concept) |
| >97 (qualifier value) |
Preferred (foundation metadata concept) |
| >= |
Preferred (foundation metadata concept) |
| ? child now: [EC69] or [EC60] from FPC] or [EC69 from HB] |
Preferred (foundation metadata concept) |
| ? child now: [EC69] or [EC60] from FPC] or [EC69 from HB] |
Preferred (foundation metadata concept) |
| ? child now: [EC69] or [EC60] from FPC] or [EC69 from HB] (finding) |
Preferred (foundation metadata concept) |
| ? child now: [EC69] or [EC60] from FPC] or [EC69 from HB] (finding) |
Preferred (foundation metadata concept) |
| ? patient now: [FP69 from FPC] or [GP69 from HB] |
Preferred (foundation metadata concept) |
| ? patient now: [FP69 from FPC] or [GP69 from HB] |
Preferred (foundation metadata concept) |
| ? patient now: [FP69 from FPC] or [GP69 from HB] (finding) |
Preferred (foundation metadata concept) |
| ? patient now: [FP69 from FPC] or [GP69 from HB] (finding) |
Preferred (foundation metadata concept) |
| A |
Preferred (foundation metadata concept) |
| A |
Preferred (foundation metadata concept) |
| A & E - Accident and Emergency Department |
Acceptable (foundation metadata concept) |
| A & E service |
Acceptable (foundation metadata concept) |
| A (tumor staging) |
Preferred (foundation metadata concept) |
| A - alphalipoproteinemia neuropathy |
Acceptable (foundation metadata concept) |
| A - ampere |
Preferred (foundation metadata concept) |
| A 102 |
Preferred (foundation metadata concept) |
| A 102 (qualifier value) |
Preferred (foundation metadata concept) |
| A Noonan-related syndrome, characterized by facial anomalies suggestive of Noonan syndrome, loose anagen hair, frequent congenital heart defects, distinctive skin features (darkly pigmented skin, keratosis pilaris, eczema or icthyosis), and short stature that is often associated with a growth hormone deficiency. Psychomotor delay with attention deficit/hyperactivity disorder (ADHD) is frequently observed. |
Preferred (foundation metadata concept) |
| A Pierre Robin syndrome associated with bone disease characterized by severe short-limbed dwarfism, joint dislocations, club feet along with distinctive facies and radiographic findings. |
Preferred (foundation metadata concept) |
| A Z-shaped cut in the first metatarsal in order to separate the head of the plantar half of the shaft from the rest of the bone. This allows the head-shaft complex to be translated and rotated in order to achieve correction of the deformity while maintaining articular congruity. |
Preferred (foundation metadata concept) |
FHIR