Disease #00932 (NBS (Nijmegen breakage syndrome (NBS)), OMIM:251260)

Official abbreviation NBS
Name Nijmegen breakage syndrome (NBS)
OMIM ID 251260
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 16
Phenotype entries for this disease 15
Associated with 1 gene NBN
Associated tissues -
Disease features cognitive delay; growth retardation; neuropsychiatric behaviors; microcephaly; craniofacial dysmorphia; cleft/arched palate; syndactyly; organ abnormalitie; no cardiac defects; limb reductions; no hearing loss; skin pigmentation abnormalities; elevated cancer incidence; no bone marrow/hematopoietic defects
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-08-31 23:31:15 +02:00 (CEST)


Individuals

16 entries on 1 page. Showing entries 1 - 16.
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00058680 - - - - - - - - - - - NBS - NBN NBN 1 1 Johan den Dunnen
00058682 - - - - - - Slavic? - - - - NBS - NBN NBN 1 46 Johan den Dunnen
00058683 - - - - - - Slavic? - - - - NBS - NBN NBN 1 46 Johan den Dunnen
00058684 - - - - - - - - - - - NBS - NBN NBN 1 1 Johan den Dunnen
00058685 - - - - - - Russian - - - - NBS - NBN NBN 1 1 Johan den Dunnen
00058686 - - - - - - English - - - - NBS - NBN NBN 1 1 Johan den Dunnen
00058687 - - - - - - Italian - - - - NBS - NBN NBN 1 1 Johan den Dunnen
00058688 - - - - - - Mexican - - - - NBS - NBN NBN 1 1 Johan den Dunnen
00058689 - - - - - - African - - - - NBS - NBN NBN 1 1 Johan den Dunnen
00058690 - - - - - - Dutch - - - - NBS - NBN NBN 1 1 Johan den Dunnen
00058691 - - - - - - - - - - - FANC, NBS Fanconi anemia, Nijmegen breakage Syndrome NBN NBN 1 1 Johan den Dunnen
00058692 - - - - - - Canadian - - - - NBS - NBN NBN 1 1 Johan den Dunnen
00058693 - - - - - - - - - - - NBS - NBN NBN 1 1 Johan den Dunnen
00058694 - - - - - - - - - - - NBS - NBN NBN 1 1 Johan den Dunnen
00295513 - - - - - - - - - - - NBS - NBN NBN 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00397937 WABS02 PubMed: van Schie 2020 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Netherlands - - - - - NBS microcephaly; sensorineural hearing loss; prenatal growth restriction; postnatal growth restriction; intellectual disability; retrognathia; skin abnormalities; cochlear abnormalities; epicanthus; no small/dysplastic ears; no brain abnormalities; seizures; feeding problems; DDX11 DDX11 2 1 Johan den Dunnen
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