Phenotypes for disease #00131 (CBAVD (vas deferens, congenital bilateral absence (CBAVD)), OMIM:277180)

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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     
0000121324 Pallido-nigro-luysian degeneration Familial 41y - - - - - - Marc Cruts 00148906
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