Phenotypes for disease #00932 (NBS (Nijmegen breakage syndrome (NBS)), OMIM:251260)

15 entries on 1 page. Showing entries 1 - 15.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000045271 - - - Unknown - - - - - Johan den Dunnen 00058680
0000045273 - - - Unknown - - - - - Johan den Dunnen 00058682
0000045274 - - - Unknown - - - - - Johan den Dunnen 00058683
0000045275 - - - Unknown - - - - - Johan den Dunnen 00058684
0000045276 - - - Unknown - - - - - Johan den Dunnen 00058685
0000045277 - - - Unknown - - - - - Johan den Dunnen 00058686
0000045278 - - - Unknown - - - - - Johan den Dunnen 00058687
0000045279 - - - Unknown - - - - - Johan den Dunnen 00058688
0000045280 - - - Unknown - - - - - Johan den Dunnen 00058689
0000045281 - - - Unknown - - - - - Johan den Dunnen 00058690
0000045282 Fanconi anemia, Nijmegen breakage Syndrome - - Unknown - - - - - Johan den Dunnen 00058691
0000045283 - - - Unknown - - - - - Johan den Dunnen 00058692
0000045284 - - - Unknown - - - - - Johan den Dunnen 00058693
0000045285 - - - Unknown - - - - - Johan den Dunnen 00058694
0000291065 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; Nijmegen Breakage Syndrome WABS Isolated (sporadic) - - - - - Johan den Dunnen 00397937
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