Disease #05208 (JBS;11q (Jacobsen syndrome (JBS; deletion syndrome, chromosome 11q)), OMIM:147791)

Official abbreviation JBS;11q
Name Jacobsen syndrome (JBS; deletion syndrome, chromosome 11q)
OMIM ID 147791
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 0 genes -
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Disease features -
Remarks -
Date created 2016-12-06 21:38:27 +01:00 (CET)
Date last edited N/A


Individuals

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00019483 - PubMed: Huizing 2001 - F no Germany;Ireland Jewish-Ashkenazi - - - - HPS, JBS;11q see paper; ... HPS3 HPS3 3 1 William (Bill) Oetting
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