Members |
acceptabilityId |
15q13.3 microduplication syndrome (disorder) |
Preferred (foundation metadata concept) |
15q14 microdeletion syndrome |
Preferred (foundation metadata concept) |
15q14 microdeletion syndrome (disorder) |
Preferred (foundation metadata concept) |
15q24 deletion |
Acceptable (foundation metadata concept) |
15q24 microdeletion |
Preferred (foundation metadata concept) |
15q24 microdeletion syndrome |
Acceptable (foundation metadata concept) |
15q26 deletion syndrome |
Acceptable (foundation metadata concept) |
15q26.3 microdeletion syndrome |
Acceptable (foundation metadata concept) |
16 |
Preferred (foundation metadata concept) |
16 (AJCC) |
Acceptable (foundation metadata concept) |
16 (UICC) |
Acceptable (foundation metadata concept) |
16 (qualifier value) |
Preferred (foundation metadata concept) |
16 Personality factor questionnaire |
Preferred (foundation metadata concept) |
16 Personality factor questionnaire (assessment scale) |
Preferred (foundation metadata concept) |
16 alpha-hydroxydehydroepiandrosterone |
Preferred (foundation metadata concept) |
16 alpha-hydroxydehydroepiandrosterone (substance) |
Preferred (foundation metadata concept) |
16 alpha-hydroxydehydroepiandrosterone sulfate |
Preferred (foundation metadata concept) |
16 alpha-hydroxydehydroepiandrosterone sulfate (substance) |
Preferred (foundation metadata concept) |
16 alpha-hydroxyestrone |
Preferred (foundation metadata concept) |
16 alpha-hydroxyestrone (substance) |
Preferred (foundation metadata concept) |
16 times a day |
Acceptable (foundation metadata concept) |
16-alpha-Hydroxypregnenolone |
Preferred (foundation metadata concept) |
16-alpha-Hydroxypregnenolone (substance) |
Preferred (foundation metadata concept) |
16-alpha-Hydroxysteroid dehydrogenase |
Preferred (foundation metadata concept) |
16-alpha-Hydroxysteroid dehydrogenase (substance) |
Preferred (foundation metadata concept) |
16-alpha-hydroxyprogesterone dehydratase |
Preferred (foundation metadata concept) |
16-alpha-hydroxyprogesterone dehydratase |
Acceptable (foundation metadata concept) |
16-alpha-hydroxyprogesterone dehydratase (substance) |
Preferred (foundation metadata concept) |
16-dehydroprogesterone hydratase |
Preferred (foundation metadata concept) |
16-dehydroprogesterone hydratase (substance) |
Preferred (foundation metadata concept) |
16-hydroxysteroid epimerase |
Preferred (foundation metadata concept) |
16-hydroxysteroid epimerase (substance) |
Preferred (foundation metadata concept) |
16-ketoandrostenediol |
Acceptable (foundation metadata concept) |
16-methoxy-2,3-dihydro-3-hydroxytabersonine N-methyltransferase |
Preferred (foundation metadata concept) |
16-methoxy-2,3-dihydro-3-hydroxytabersonine N-methyltransferase (substance) |
Preferred (foundation metadata concept) |
16-oxoandrostenediol |
Preferred (foundation metadata concept) |
16-oxoandrostenediol (substance) |
Preferred (foundation metadata concept) |
16.1 |
Preferred (foundation metadata concept) |
16.1 (qualifier value) |
Preferred (foundation metadata concept) |
16.2 |
Preferred (foundation metadata concept) |
16.2 (qualifier value) |
Preferred (foundation metadata concept) |
16.58 |
Preferred (foundation metadata concept) |
16.58 (qualifier value) |
Preferred (foundation metadata concept) |
16.7 |
Preferred (foundation metadata concept) |
16.7 (qualifier value) |
Preferred (foundation metadata concept) |
16.8 |
Preferred (foundation metadata concept) |
16.8 (qualifier value) |
Preferred (foundation metadata concept) |
16/16 |
Preferred (foundation metadata concept) |
16/22 |
Preferred (foundation metadata concept) |
160 |
Preferred (foundation metadata concept) |
160 (qualifier value) |
Preferred (foundation metadata concept) |
1600 |
Preferred (foundation metadata concept) |
1600 (qualifier value) |
Preferred (foundation metadata concept) |
16000 |
Preferred (foundation metadata concept) |
16000 (qualifier value) |
Preferred (foundation metadata concept) |
162 |
Preferred (foundation metadata concept) |
162 (qualifier value) |
Preferred (foundation metadata concept) |
1627 Burgas |
Preferred (foundation metadata concept) |
164-Yb |
Acceptable (foundation metadata concept) |
165 |
Preferred (foundation metadata concept) |
165 (qualifier value) |
Preferred (foundation metadata concept) |
166 |
Preferred (foundation metadata concept) |
166 (qualifier value) |
Preferred (foundation metadata concept) |
166-Ho |
Acceptable (foundation metadata concept) |
166-Yb |
Acceptable (foundation metadata concept) |
166.667 |
Preferred (foundation metadata concept) |
166.667 (qualifier value) |
Preferred (foundation metadata concept) |
16600 |
Preferred (foundation metadata concept) |
16600 (qualifier value) |
Preferred (foundation metadata concept) |
16667 |
Preferred (foundation metadata concept) |
16667 (qualifier value) |
Preferred (foundation metadata concept) |
1667 |
Preferred (foundation metadata concept) |
1667 (qualifier value) |
Preferred (foundation metadata concept) |
167 |
Preferred (foundation metadata concept) |
167 (qualifier value) |
Preferred (foundation metadata concept) |
168 |
Preferred (foundation metadata concept) |
168 (qualifier value) |
Preferred (foundation metadata concept) |
1680 |
Preferred (foundation metadata concept) |
1680 (qualifier value) |
Preferred (foundation metadata concept) |
16800 |
Preferred (foundation metadata concept) |
16800 (qualifier value) |
Preferred (foundation metadata concept) |
169-Er |
Acceptable (foundation metadata concept) |
169-Hf |
Acceptable (foundation metadata concept) |
169-Yb |
Acceptable (foundation metadata concept) |
16G |
Preferred (foundation metadata concept) |
16G (qualifier value) |
Preferred (foundation metadata concept) |
16PF - Personality factor questionnaire |
Acceptable (foundation metadata concept) |
16p partial trisomy syndrome |
Preferred (foundation metadata concept) |
16p partial trisomy syndrome (disorder) |
Preferred (foundation metadata concept) |
16p11.2 deletion syndrome |
Acceptable (foundation metadata concept) |
16p11.2p12.2 microdeletion syndrome |
Preferred (foundation metadata concept) |
16p11.2p12.2 microdeletion syndrome (disorder) |
Preferred (foundation metadata concept) |
16p11.2p12.2 microduplication syndrome |
Preferred (foundation metadata concept) |
16p11.2p12.2 microduplication syndrome (disorder) |
Preferred (foundation metadata concept) |
16p12.1p12.3 triplication syndrome |
Preferred (foundation metadata concept) |
16p12.1p12.3 triplication syndrome (disorder) |
Preferred (foundation metadata concept) |
16p12.1p12.3 triplication syndrome is a rare chromosomal anomaly syndrome resulting from the partial triplication of the short arm of chromosome 16 characterized by global developmental delay, pre- or post-natal growth delay and distinctive craniofacial features, including short palpebral fissures, epicanthal folds, bulbous nose, thin upper vermillion border, apparently low-set ears and large ear lobes. Variable clinical features that have been reported include congenital heart disease, genitourinary abnormalities, visual anomalies or, less commonly, infantile hepatic disease. Patients are also reported to have tapered fingers. |
Preferred (foundation metadata concept) |
16p12.2 microdeletion |
Acceptable (foundation metadata concept) |
16p12.2 microdeletion syndrome |
Preferred (foundation metadata concept) |
16p12.2 microdeletion syndrome (disorder) |
Preferred (foundation metadata concept) |
16p13.11 microdeletion syndrome |
Preferred (foundation metadata concept) |