| Members |
acceptabilityId |
| 830 (qualifier value) |
Preferred (foundation metadata concept) |
| 833 |
Preferred (foundation metadata concept) |
| 833 (qualifier value) |
Preferred (foundation metadata concept) |
| 833.33 |
Preferred (foundation metadata concept) |
| 833.33 (qualifier value) |
Preferred (foundation metadata concept) |
| 833.333 |
Preferred (foundation metadata concept) |
| 833.333 (qualifier value) |
Preferred (foundation metadata concept) |
| 83m-Kr |
Acceptable (foundation metadata concept) |
| 84 |
Preferred (foundation metadata concept) |
| 84 (qualifier value) |
Preferred (foundation metadata concept) |
| 84-Rb |
Acceptable (foundation metadata concept) |
| 84.75 |
Preferred (foundation metadata concept) |
| 84.75 (qualifier value) |
Preferred (foundation metadata concept) |
| 840 |
Preferred (foundation metadata concept) |
| 840 (qualifier value) |
Preferred (foundation metadata concept) |
| 85 |
Preferred (foundation metadata concept) |
| 85 (qualifier value) |
Preferred (foundation metadata concept) |
| 85-Kr |
Acceptable (foundation metadata concept) |
| 85-Sr |
Acceptable (foundation metadata concept) |
| 85-Y |
Acceptable (foundation metadata concept) |
| 850 |
Preferred (foundation metadata concept) |
| 850 (qualifier value) |
Preferred (foundation metadata concept) |
| 8500 |
Preferred (foundation metadata concept) |
| 8500 (qualifier value) |
Preferred (foundation metadata concept) |
| 856 |
Preferred (foundation metadata concept) |
| 856 (qualifier value) |
Preferred (foundation metadata concept) |
| 85m-Kr |
Acceptable (foundation metadata concept) |
| 85m-Sr |
Acceptable (foundation metadata concept) |
| 85m-Y |
Acceptable (foundation metadata concept) |
| 86-Rb |
Acceptable (foundation metadata concept) |
| 86-Y |
Acceptable (foundation metadata concept) |
| 86-Zr |
Acceptable (foundation metadata concept) |
| 87 |
Preferred (foundation metadata concept) |
| 87 (qualifier value) |
Preferred (foundation metadata concept) |
| 87-Kr |
Acceptable (foundation metadata concept) |
| 87-Rb |
Acceptable (foundation metadata concept) |
| 87-Y |
Acceptable (foundation metadata concept) |
| 87-Zr |
Acceptable (foundation metadata concept) |
| 87.5 |
Preferred (foundation metadata concept) |
| 87.5 (qualifier value) |
Preferred (foundation metadata concept) |
| 875 |
Preferred (foundation metadata concept) |
| 875 (qualifier value) |
Preferred (foundation metadata concept) |
| 87m-Sr |
Acceptable (foundation metadata concept) |
| 87m-Y |
Acceptable (foundation metadata concept) |
| 88 |
Preferred (foundation metadata concept) |
| 88 (qualifier value) |
Preferred (foundation metadata concept) |
| 88-Kr |
Acceptable (foundation metadata concept) |
| 88-Rb |
Acceptable (foundation metadata concept) |
| 88-Y |
Acceptable (foundation metadata concept) |
| 88-Zr |
Acceptable (foundation metadata concept) |
| 89-Sr |
Acceptable (foundation metadata concept) |
| 89-Zr |
Acceptable (foundation metadata concept) |
| 8Fr |
Acceptable (foundation metadata concept) |
| 8G |
Preferred (foundation metadata concept) |
| 8G (qualifier value) |
Preferred (foundation metadata concept) |
| 8p inverted duplication deletion syndrome |
Preferred (foundation metadata concept) |
| 8p inverted duplication deletion syndrome (disorder) |
Preferred (foundation metadata concept) |
| 8p partial monosomy syndrome |
Preferred (foundation metadata concept) |
| 8p partial monosomy syndrome (disorder) |
Preferred (foundation metadata concept) |
| 8p partial trisomy syndrome |
Preferred (foundation metadata concept) |
| 8p partial trisomy syndrome (disorder) |
Preferred (foundation metadata concept) |
| 8p11.2 deletion syndrome |
Preferred (foundation metadata concept) |
| 8p11.2 deletion syndrome (disorder) |
Preferred (foundation metadata concept) |
| 8p11.2 deletion syndrome is a contiguous gene syndrome characterised by the association of congenital spherocytosis, dysmorphic features, growth delay and hypogonadotropic hypogonadism. |
Preferred (foundation metadata concept) |
| 8p23.1 deletion involves a partial deletion of the short arm of chromosome 8 characterised by low birth weight, postnatal growth deficiency, mild intellectual deficit, hyperactivity, craniofacial abnormalities, and congenital heart defects. |
Preferred (foundation metadata concept) |
| 8p23.1 duplication syndrome |
Preferred (foundation metadata concept) |
| 8p23.1 duplication syndrome (disorder) |
Preferred (foundation metadata concept) |
| 8p23.1 duplication syndrome is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the short arm of chromosome 8, with a highly variable phenotype, principally characterised by mild to moderate developmental delay, intellectual disability, mild facial dysmorphism (including prominent forehead, arched eyebrows, broad nasal bridge, upturned nares, cleft lip and/or palate) and congenital cardiac anomalies (e.g., atrioventricular septal defect). Other reported features include macrocephaly, behavioural abnormalities (e.g., attention deficit disorder), seizures, hypotonia and ocular and digital anomalies (poly/syndactyly). |
Preferred (foundation metadata concept) |
| 8p23.1 microdeletion syndrome |
Preferred (foundation metadata concept) |
| 8p23.1 microdeletion syndrome (disorder) |
Preferred (foundation metadata concept) |
| 8q partial monosomy syndrome |
Preferred (foundation metadata concept) |
| 8q partial monosomy syndrome (disorder) |
Preferred (foundation metadata concept) |
| 8q partial trisomy syndrome |
Preferred (foundation metadata concept) |
| 8q partial trisomy syndrome (disorder) |
Preferred (foundation metadata concept) |
| 8q12 microduplication syndrome |
Preferred (foundation metadata concept) |
| 8q12 microduplication syndrome (disorder) |
Preferred (foundation metadata concept) |
| 8q13 microdeletion syndrome |
Preferred (foundation metadata concept) |
| 8q13 microdeletion syndrome (disorder) |
Preferred (foundation metadata concept) |
| 8q21.11 microdeletion syndrome |
Preferred (foundation metadata concept) |
| 8q21.11 microdeletion syndrome (disorder) |
Preferred (foundation metadata concept) |
| 8q21.11 microdeletion syndrome encompasses heterozygous overlapping microdeletions on chromosome 8q21.11 resulting in intellectual disability, facial dysmorphism comprising a round face, ptosis, short philtrum, Cupid's bow and prominent low-set ears, nasal speech and mild finger and toe anomalies. |
Preferred (foundation metadata concept) |
| 8q22.1 microdeletion syndrome |
Preferred (foundation metadata concept) |
| 8q22.1 microdeletion syndrome (disorder) |
Preferred (foundation metadata concept) |
| 8q24.3 microdeletion syndrome |
Preferred (foundation metadata concept) |
| 8q24.3 microdeletion syndrome (disorder) |
Preferred (foundation metadata concept) |
| 8th floor |
Acceptable (foundation metadata concept) |
| 9 |
Preferred (foundation metadata concept) |
| 9 |
Preferred (foundation metadata concept) |
| 9 (qualifier value) |
Preferred (foundation metadata concept) |
| 9 French gauge |
Preferred (foundation metadata concept) |
| 9 French gauge (qualifier value) |
Preferred (foundation metadata concept) |
| 9 cis-hexadecenoic acid |
Acceptable (foundation metadata concept) |
| 9 cis-octadecenoic acid |
Preferred (foundation metadata concept) |
| 9 cis-octadecenoic acid (substance) |
Preferred (foundation metadata concept) |
| 9 cis-octadecenoic acid and oil of turpentine only product |
Preferred (foundation metadata concept) |
| 9 cis-octadecenoic acid only product |
Preferred (foundation metadata concept) |
| 9 cis-octadecenoic acid- and oil of turpentine-containing product |
Preferred (foundation metadata concept) |
| 9 cis-octadecenoic acid-containing product |
Preferred (foundation metadata concept) |
| 9 mm caliber bullet, device |
Acceptable (foundation metadata concept) |
| 9 mm caliber bullet, device (physical object) |
Preferred (foundation metadata concept) |
| 9 mm calibre bullet |
Preferred (foundation metadata concept) |
FHIR