Jacobsen syndrome
(Q1677755)
multiple congenital anomaly caused by deletion on chromosome 11
multiple congenital anomaly caused by deletion on chromosome 11
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Current Data About
Jacobsen syndrome
| (P18) |
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| (P31) |
(Q929833)
(Q55788864)
(Q112193867) (Q112965645) |
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| (P61) |
(Q23781981)
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| (P279) |
(Q55788346)
(Q622427)
(Q55786613)
(Q16918398)
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| (P373) |
Jacobsen syndrome
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| (P667) |
A90
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| (P1748) |
C75457
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| (P1995) |
(Q1071953)
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| (P2888) |
http://www.orpha.net/ORDO/Orphanet_2308
http://purl.obolibrary.org/obo/DOID_0111723
http://identifiers.org/doid/DOID:0111723
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other details
| aliases |
Partial 11Q Monosomy Syndrome JBS JACOBSEN SYNDROME Distal monosomy 11q Chromosome 11Q Deletion Syndrome Distal deletion 11q Monosomy 11qter JACOBSEN SYNDROME; JBS Del(11)(qter) Telomeric deletion 11q 11q Terminal Deletion Disorder Del(11)(q23.3) Jacobsen Syndrome Jacobsen Distal 11q Deletion Syndrome |
| description | multiple congenital anomaly caused by deletion on chromosome 11 |
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