Contiguous gene deletion syndrome
Symptom Information:
| Symptom ID: | OMIM : No Id available | |
| Synonyms: |
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MedDRA: |
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| Database Frequency: | 23 / 7739 | |
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All diseases associated with this symptom:
| 14q11.2 microdeletion syndrome | (Orphanet:261120) |
| 15q24 microdeletion syndrome | (Orphanet:94065) |
| 17q11 microdeletion syndrome | (Orphanet:97685) |
| 17q11.2 microduplication syndrome | (Orphanet:139474) |
| 17q12 microdeletion syndrome | (Orphanet:261265) |
| 19q13.11 microdeletion syndrome | (Orphanet:217346) |
| 1p36 deletion syndrome | (Orphanet:1606) |
| 1q41q42 microdeletion syndrome | (Orphanet:250999) |
| 2q32q33 microdeletion syndrome | (Orphanet:251019) |
| 3q29 microdeletion syndrome | (Orphanet:65286) |
| 4q21 microdeletion syndrome | (Orphanet:238750) |
| 8q21.11 microdeletion syndrome | (Orphanet:284160) |
| CHROMOSOME 16q22 DELETION SYNDROME | (OMIM:614541) |
| CHROMOSOME 17p13.1 DELETION SYNDROME | (OMIM:613776) |
| CHROMOSOME 1p32-p31 DELETION SYNDROME | (OMIM:613735) |
| CHROMOSOME 6q11-q14 DELETION SYNDROMECHROMOSOME 6q13-q14 DELETION SYNDROME, INCLUDED | (OMIM:613544) |
| Choroideremia - deafness - obesity | (Orphanet:1435) |
| Distal monosomy 10q | (Orphanet:96148) |
| Distal monosomy 3p | (Orphanet:1620) |
| Jacobsen syndrome | (Orphanet:2308) |
| Monosomy 13q14 | (Orphanet:1587) |
| Monosomy 18p | (Orphanet:1598) |
| Wolf-Hirschhorn syndrome | (Orphanet:280) |