Phenotypes for disease #00166 (NBSLD (Nijmegen breakage syndrome-like disorder (NBSLD)), OMIM:613078)

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AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Phenotype details     

Protein     

Owner     

Individual ID     
0000021602 - Isolated (sporadic) - - - - - - - Najim Ameziane 00001616
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