Phenotypes for disease #01126 (MRXSN (mental retardation, X-linked syndromic, Nascimento-type (MRXSN)), OMIM:300860)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Birth_Details     

Protein     

Owner     

Individual ID     
0000228643 - - - Familial, X-linked recessive - 35y - - - - Giulio Piluso 00301513
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