Phenotypes for disease #01018 (CSS4;MRD16 (Coffin-Siris syndrome, type 4 (CSS4, mental retardation, autosomal dominant syndrome, type 16 (MRD16))), OMIM:614609)

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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     
0000274628 DD; coarse face; encephalocele; omphalocele; bifid uvula; sub mucous cleft palate; ataxia; muscular hypotonia (Multiple system disease) - Coffin-Siris type 4 Familial - - - - - LOVD 00380775
0000326676 feeding difficulties - CSS syndrome Unknown 1month - - - - Jing Mou 00436445
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