Phenotypes for disease #05268 (SCKL1 (Seckel syndrome, type 1), OMIM:210600)

5 entries on 1 page. Showing entries 1 - 5.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000090170 Mild intellectual disability - - Unknown - - - - Emmelien Aten 00114688
0000090174 Mild intellectual disability - - Unknown - - - - Emmelien Aten 00114692
0000090178 - - - Unknown - - - - Emmelien Aten 00114696
0000090179 intellectual disability - - Unknown - - - - Emmelien Aten 00114697
0000090181 - - - Unknown - - - - Emmelien Aten 00114699
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