Phenotypes for disease #05159 (MRXS34 (mental retardation, X-linked, syndromic, type 34), OMIM:300967)

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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     
0000309682 tricuspid regurgitation; abnormal myocardium morphology; ventricular septal defect; anemia; hepatic hemangioma; postnatal growth retardation; noncompaction cardiomyopathy, atrial septal defect - - Familial, X-linked recessive - - - - - Xiaoyan Peng 00417862
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