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loading...| Preferred Name |
Chromosome 17q21.31 Deletion Syndrome |
| Synonyms |
Monosomy 17q21.31 |
| ID |
http://purl.bioontology.org/ontology/MESH/C566476 |
| altLabel |
Monosomy 17q21.31 17q21.31 Deletion Syndrome Koolen Syndrome Microdeletion 17q21.31 Syndrome Chromosome 17q21.31 Microdeletion Syndrome 17q21.31 Microdeletion Syndrome Koolen-De Vries Syndrome |
| cui |
C1864871 |
| HM |
D002886 D008607 D002872 D000015 |
| Inverse of RB |
0 |
| Mapped to |
http://purl.bioontology.org/ontology/MESH/D002872 http://purl.bioontology.org/ontology/MESH/D008607 |
| MDA |
20121105 |
| MeSH Frequency |
22 |
| MMR |
20131024 |
| notation |
C566476 |
| prefLabel |
Chromosome 17q21.31 Deletion Syndrome |
| SC |
3 |
| TERMUI |
T840733 T840731 T840730 T840735 T808582 T840734 T808583 T840732 |
| TH |
OMIM (2013) GHR (2014) |
| tui |
T047 |
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| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/OMIM/612452 | Online Mendelian Inheritance in Man | CUI | |
| http://purl.bioontology.org/ontology/OMIM/610443 | Online Mendelian Inheritance in Man | CUI |