Phenotypes for disease #04666 (MRT48 (mental retardation, autosomal recessive, type 48 (MRT-48)), OMIM:616269)

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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     
0000351312 intellectual disbaility, short stature, developmental delay MRT48 intellectual disbaility Familial, autosomal recessive 01y 01y 00y 0y - Malik Ali Asghar 00465863
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