| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Complete trisomy 8 syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| anomalie du chromosome 12 (trouble) | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Penta X syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| XY, female phenotype | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Ring chromosome 22 syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Partial trisomy 21 in Down's syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Karyotype 46, X iso (Xq) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Male with sex chromosome mosaicism | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Turner's phenotype, partial X deletion karyotype | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Complete trisomy 13 syndrome | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Trisomy 18 - mitotic nondisjunction mosaicism | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Anomaly of chromosome pair 19 | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| 22q11.2 duplication syndrome (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Mosaicism - lines with various numbers of X chromosomes | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| 21q partial distal trisomy (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Klinefelter's syndrome, XXY (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Male with structurally abnormal sex chromosome | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Turner's phenotype - ring chromosome karyotype | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Trisomy 21- meiotic nondisjunction | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Complete trisomy 20 syndrome (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Complete trisomy 16 syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Trisomy 18 - meiotic nondisjunction | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Klinefelter's syndrome XXXY | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Klinefelter's syndrome XXXXY | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Mosaic XO/XX | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Congenital hereditary endothelial dystrophy type 1 (disorder) | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 2 | 
| tétrasomie 12p (trouble) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Anomaly of chromosome X | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Sex phenotype-karyotype dissociation syndrome | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Angelman syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 3 | 
| FRAXA | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| anomalie du chromosome 22 | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Mixed gonadal dysgenesis | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 2 | 
| anomalie du chromosome 7 (trouble) | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Ring chromosome 18 syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Additional sex chromosome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Sex chromosome mosaicism | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Double Y syndrome (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| XXXY syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| anomalie du chromosome 9 (trouble) | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Café-au-lait spots and ring chromosome 11 (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Trisomy 21- mitotic nondisjunction mosaicism | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Anomaly of chromosome pair 11 | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| syndrome de chromosome 9 en anneau | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Fragile X chromosome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Anomaly of chromosome pair 4 | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| 15q24 microdeletion | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Trisomy 13, meiotic nondisjunction | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| dystrophie endothéliale congénitale héréditaire type II | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 2 | 
| Klinefelter syndrome, male with 46,XX karyotype (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| 15q13.3 microdeletion | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Mosaicism 45, X; 46, XX | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Mosaic XY/XXY | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| 22q13.3 deletion syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Trisomy 13 - mitotic nondisjunction mosaicism | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| 21q partial trisomy (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| XY females | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| anomalie du chromosome 18 (trouble) | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Mosaicism 45, X / other cell line with abnormal sex chromosome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Four X syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Anomaly of chromosome pair 1 | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| 11p partial monosomy syndrome (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 2 | 
| Klinefelter's syndrome, XXYY | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Klinefelter's syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| anomalie du chromosome 16 (trouble) | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Tetrasomy 18p | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| 1q21.1 microdeletion | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| FRAXE | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Klinefelter's syndrome, XY/XXY mosaic | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| syndrome du chromosome 1 en anneau (trouble) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Anomaly of sex chromosome | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Ulnar mammary syndrome | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Chromosome 2q37 deletion syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Fetus with complete trisomy 13 syndrome (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 3 | 
| Fetus with complete trisomy 18 syndrome (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 3 | 
| Fetus with complete trisomy 21 syndrome (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 3 | 
| Fetus with Turner syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 3 | 
| Prader-Willi syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Williams syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 2 | 
| Potocki-Shaffer syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 6 | 
| Deletion of part of autosome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Autosomal deletion - mosaicism | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Whole chromosome monosomy - mitotic nondisjunction mosaicism | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| 22q11 partial monosomy syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Monosomy 21, mosaicism | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Deletion of long arm of chromosome 18 | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Monosomy and deletion from autosome | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Deletion with complex rearrangement | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Deletion of long arm of chromosome 13 | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Whole chromosome monosomy - meiotic nondisjunction | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Deletion seen only at prometaphase | morphologie associée (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Deletion of short arm of chromosome 18 | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Dual red blood cell population | est un(e) (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some |  | 
| Periodontitis co-occurrent with Down syndrome | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 3 | 
| Chromosome 11p13 deletion syndrome (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 2 | 
| Tetrasomy of short arm of chromosome 9 (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 2 | 
| Maternal uniparental disomy of chromosome 20 (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Paternal uniparental disomy of chromosome 20 (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Deletion of long arm of chromosome 17 (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 1 | 
| Koolen De Vries syndrome (disorder) | morphologie associée (attribut) | False | Cellular AND/OR subcellular abnormality | Inferred relationship | Some | 3 | 
| Aggregated spermatozoa (morphologic abnormality) | est un(e) (attribut) | True | Cellular AND/OR subcellular abnormality | Inferred relationship | Some |  |