Phenotypes for disease #02170 (BRNRS (Brunner syndrome (BRNRS, monoamine oxidase A deficiency)), OMIM:300615)

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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     
0000087493 Male, 7 y, speech delay, moderate ID, behavioral anomalies (maternal XI 82%) - - Familial, X-linked recessive - - - - - Bernt Popp 00111408
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